藥物成份

共有 21647 個藥物成份

The NOR Partigen* immunodiffusion plate contains monospecific antiserum to the respective human protein in a layer of agarose gel.

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The NOR Partigen* immunodiffusion plate contains monospecific antiserum to the respective human protein in a layer of agarose gel. The antisera are obtained by immunizing rabbits (R) or sheep (S).Preservative: Sodium azide <1g/L, sodium timerfonate <0.025g/L

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The PE conjugate is supplied as 25ug in 1.0mL(25ug/mL) of phosphate-buffered saline(PBS). \nPBS contains gelatin and 0.1% sodium azide.\nTwenty microliters (20uL) of the PE-conjugated antibody stains 10X6 peripheral blood mononuclear cells(PBMCs)\n

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The PMIC/ID panel contains the antimicrobial agents (ug/mL)\n Amoxicillin/Clavulanate(1/0.5 –4/2), Ampicillin(0.25 - 8),Beta-Lactamase ( <10), Cefazolin(2 – 16), Cefotaxime(8 – 32), Cefuroxime(4 – 16), Ciprofloxacin(0.5 – 2), Clindamycin (0.5 – 2),Erythtomycin (0.25 – 4),Fusidic Acid (1-8), Gentamicin(2 – 8), Gentamicin-Sunergy (500), Levofloxacin(1 – 4), Linezolid (1-4), Nitrofurantoin(16 – 64),Oxacillin (0.25- 4), Penicillin (0.06 –8), Quinupristin/Dalfopristin (0.5 – 4), Rifampin (0.5 – 2),Streptomycin-Synergy (1000), Tetracycline(0.5 –8),Trimethoprim/Sulfamethoxazole (0.5/9.5 – 2/38), Vancomycin (1 – 16) \n\n

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The PST Blood Collection Tubes contain anticoagulant of Heparin.

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The SMIC/ID panel contains the antimicrobial agents (ug/mL)\n Amoxicillin/Clavulanate(0.25/0.125 - 4/2), Ampicillin(0.25 - 4), \n Cefepime(0.25 - 2), Cefotaxime(0.25 - 2), \n Ceftriaxone(0.25 - 2), Cefuroxime(0.25 - 2), \n Chloramphenicol(2 - 8), Clindamycin (0.03125 – 0.5), Erythromycin (0.0625 – 0.5), Gatifloxacin (0.25 – 2), Imipenem(0.0625 - 2), \n Levofloxacin(0.5 – 4), Meropenem(0.0625 - 2), Penicillin (0.0625 – 4), Telithromycin (0.0625 – 2), Tetracycline (0.5 – 8), Trimethoprim/Sulfamethoxazole (0.5/9.5 – 2/38), Vancomycin (0.25 – 1)\n \n\n

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The SMIC/ID panel contains the antimicrobial agents (ug/mL)\nAmoxicillin(0.25-4), Cefepime(0.5-2), Cefotaxime(0.5-4), Chloramphenicol(2-8), Clindamycin(0.03125-2), Erythromycin(0.0625-4), Gentamicin-Syn(250-1000), Levofloxacin(0.5-4), Linezolid(1-4), Meropenem(0.125-0.5), Moxifloxacin(0.25-2), Penicillin(0.03125-8), Pristinamycin(0.25-2), Teicoplanin(1-8), Telithromycin(0.0625-2), Tetracycline(0.5-8), Trimethoprim/Sulfamethoxazole(0.5/9.5-2/38), Vancomycin(0.5-8)處方變更為：空白。

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The Salmonella somatic antisera are preserved with 0.5% phenol and the Salmonella flagellar antisera with 0.02% thiomersal. The sera are produced in rabbits.

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The Specific Proteins Multiconstituent Calibrator (SProt Multi Cal) is prepared from human lgA, lgG, lgM, C3, C4, haptoglobin, and transferrin fractions in humen serum.

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The TB Reagents included：Carbolfuchsin、Decolorizer、Potassium Permanganate、Auramine M、Auramine -Rhodamine....stains。

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The Terasaki HLA Class I and Class II Typing Trays contain known Class I or Class II alloantisera or monoclonal antibodies. Each well contains 1 ul of antibody and 5 ul of heavy mineral oil. Sources of monoclonal may be mouse or human.

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The Urinary/Cerebrospinal Fluid Protein Calibrator is a saline solution containing human serum albumin and IgG. It consists of 10 vials, 2 each of 5 levels.

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The VITROS DT Calibrators (3 vials each of lyophilized calibrator 1, 2, 3 and 4) are prepared from bovine serum albumin and processed bovine serum to which enzymes, electrolytes, stabilizers, preservatives and other organic analytes have been added.\nVITROS DT Calibrator Diluents (3 vials each of calibrator diluent 1,2,3 and 4 containing 5 mL) are prepared from processed water to which inorganic salts have been added.

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The YBC card contains 30 wells. Of these, 26 contain biochemical broths, and four contain negative control broths.

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The antibody is diluted in 0.05 M Tris buffered saline, 0.01 M EDTA, 0.05% Brij-35 with 0.3% carrier protein and 0.05% sodium azide, a preservative. There is trace fetal calf serum, approximately 0.25%, present from the stock solution.

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The bovine albumin solutions with a protein concentration of 22%, specifically designed for serological use. The pH is 7.2.\nThe reagents contain 0.1% sodium azide as a preservative.

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The calibration sera are based on lyophilised human serum and available at 2 levels.

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The calibrator contains human urine and preservative.

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The calibrator contains nordiazepam, verified by gas chromatoraphy/mass spectroscopy (GC/MS), at a target concentration of 300 ng/ml.

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The calibrator is derived from fresh frozen human plasma that has been defibrinatedand processed.

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The calibrator is prepared form processed human serum.

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The calibrator is prepared from human urine to which drugs of abuse, metabolites of drugs of abuse, organic salt, surfactants, and preservative have been added.

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The calibrator is prepared from processed human serum to which purified human C-reactive protein, inorganic salts, and preservatives have been added (Calibrator Vial 1 contains CRP 0.7mg/dL or 7mg/L; Calibrator Vial 2 contains CRP 2.5mg/dL or 25mg/L; Calibrator Vial 3 contains CRP10.0mg/dL or 100mg/L).

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The calibrator is prepared from purified human pancreatic lipase.

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The calibrators contain human urine, \nBenzoylecgonine, \nEDDP, d-Methamphetamine, \nMorphine, Nitrazeparn, \nPhencyclidine, and\nSecobarbital.

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The calibrators is derived from frozen human plasma that has been defibrinated and processed.

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The calibrators/controls contain the following stated drug concentrations (level 0- level 1- level 2- level 3- level 4- level 5) at ng/mL:\nBenzoylecgonine: 0-0-150-300-500-1000\nLormetazepam: 0-0-100-200-300-1000\nMethadone: 0-0-150-300-500-1000\nD-Methamphetamine: 0-300-500-1000-0-2000\nMethaqualone: 0-0-150-300-500-1000\nMorphine: 0-300-1000-2000-0-4000\n11-nor-&#8710;9-THC-9-COOH: 0-0-20-50-100-200\nPhencyclidine: 0-0-12.5-25-75-100\nPropoxyphene: 0-0-150-300-500-1000\nSecobarbital: 0-0-100-200-300-800\n\n

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The cartridge contains solutions with the following approximate concentrations:\nPC Solution A \npH 6.90 organic buffer; pCO2 = 64 mmHg, pO2 = 115 mmHg, Na+ = 105 mmol/L, K+ = 7.1 mmol/L, Ca++ = 1.8 mmol/L, Cl- = 48 mmol/L, glucose = 144 mg/dL, lactate = 3.3 mmol/L, tHb = 14.5 g/dL, O2Hb = 89.5%, COHb = 2.5%, MetHb = 1.5%, HHb = 6.5%, Hct = 28%, surfactant and inert preservative

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The concentration of SHBG Cal1 is approx. 0nmol/L; SHBG Cal2 contains approx. 40 nmol/L human SHBG in a human serum matrix.

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The concentrations and activities of the components are lot-specific.

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The control contains pooled human serum with 0.1% sodium azide as preservative

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The control is a lyophilozed control prepared from human serum.

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The control is made of lyophilized citrated sheep plasma and erythrocytes.

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The control serum (Human) contains, Acid phosphatase (Human seminal plasma), \nAlkaline phosphatase (Bovine intestine), Amylase (Porcine pancreas), CK (Porcine heart), \nGOT (Porcine heart), GPT (Porcine heart), γ-GTP (Bovine kidney), LDH (Chicken heart), and Lipase (Porcine pancreas).

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The device contains anti-a HCG antibody and anti-B HCG antibody at each concentration of 5 mg/mL.

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The diluent used for these low protein reagents contains sodium chloride, bovine serum albumin, a buffer and other selected components to enhance the performance of the reagent. Sodium azide, at a final concentration of 0.1%, is added as an antimicrobial agent.

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The enhancement Solution is a ready-for-use solution with Triton X-100, acetic acid and chelators.

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The filter membrane pre-coated with Anti-hLH Ab.

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The final concentration of nonantibody reagents when reconstituted to 500μL is 0.2% gelatin,0.01M potassium phosphate,0.15M NaCl,and 0.1% NaN3.

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The following are included in Directigen EZ RSV kit Directigen EZ RSV Devices 30 Each device containing a control line of inactivated RSV antigen and a test line of monoclonal RSV antibody on the membrane. Extraction Reagent E 4.0 mL Extraction, 4% mucolytic agent and 16% detergent, with 0.2% sodium azide (preservative) Control+ 2.0 mL Positive Control, detergent-treated RSV infected HEp-2 cells with 0.1% sodium azide (preservative). Control- 2.0 mL negative Control, detergent-treateed non-infected Hep-2 cells, with 0.1% sodium azide (preservative) DispensTubeTM Tubes 30 Tubes for specimen extraction and sample deliveryinto device. DispensTube Tips 30 Tips to filter sample when delivered into device.

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The gold conjugate reagents labeled with Anti-hLH Ab.

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The interior of the MiniCollect tube wall is coated with either dipotassium EDTA (K2EDTA) or tripotassium EDTA (K3EDTA).

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The kit contains one each lyophilized vials of isoniazid and rifampin and four vials of SIRE Supplement. \nApproximate Formula Per Vial Lyophilized drug: Isoniazid.....33.2 μg、\nApproximate Formula Per Vial Lyophilized drug: Rifampin.....332 μg

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The kit contains one each lyophilized vials of streptomycin, isoniazid, rifampin and ethambutol and eight vials of SIRE Supplement.Approximate Formula Per Vial Lyophilized drug: Streptomycin……..332μgApproximate Formula Per Vial Lyophilized drug: Isoniazid………….33.2μgApproximate Formula Per Vial Lyophilized drug: Rifampin………….332μgApproximate Formula Per Vial Lyophilized drug: Ethanbutol……….1660μg

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The kit contains one vial Lyophilized streptomycin and two vials of SIRE Surpplement.\nApproximate Formula* Per Vial Lyophilized drug: Streptomycin.................664 μg

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The kit contains one vial lyophilized isoniazid and two\nvials of SIRE Supplement.\nApproximate Formula Per Vial Lyophilized drug：Isoniazid.........66.4ug

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The lyophilized HDL Calibrator is prepared from human serum.

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The matrix for the UTAK Bi-Level AED II Control is prepared from normal human serum. The analytes are adjusted to the desired concentration range for each lot prepared. Quality control bofore, during, and after the preparation of the control material ensure that each lot is of the same quality.

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The matrix for the UTAK Bi-Level Trace Elements Control is prepare from normal human whole blood. The metal concentrations are adjusted to the desired concentration range for each lot prepared. Quality control before, during, and after the preparation of the control material ensure that each lot is of the same quality.

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The matrix for the UTAK Four-Level Lead Control is prepared from normal human whole blood. The metal concentrations are adjusted to the desired concentration range for each lot prepared. Quality control before, during, and after the preparation of the control material ensure that each lot is of the same quality.

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The matrix for the UTAK Homocysteine Control is prepare from normal human whole blood.

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The matrix for the UTAK Metals is prepared from normal human whole blood. The metal concentrations are adjusted to the desired concentration range for each lot prepared. Quality control before, during, and after the preparation of the control material ensure that each lot is of the same quality.

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The matrix for the UTAK Tri-Level Immunosuppressants Control is prepared from normal human whole blood. The analytes are added and adjusted to the desired concentration range for each lot prepared.

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The matrix is prepared from normal human whole blood. The analytes are added and adjusted to the desired concentration range for each lot prepared. Quality control before, during, and after the preparation of the control material ensures that each lot is of the same quality.

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The medium tube contains 110 μL of fluorescent indicator and 7 mL of PZA broth. The pH is adjusted to 5.9. \nApproximate Formula Per L of Purified Water:\nModified Middlebrook 7H9 broth 5.9g\nCasein peptone 1.25g\nKit contains two lyophilized vials of pyrazinamide and six vials of PZA Supplement.\nApproximate Formula Per Vial Lyophilized drug: Pyrazinamide 20000 μg\nSupplement contains 15 mL of enrichment\nApproximate Formula Per L Purified Water: \nBovine albumin 50.0g\nDextrose 20.0g\nPolyoxyethylene stearate (POES) 1.1g \nCatalase 0.03g\nOleic Acid 0.1g\n

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The monoclonal antibody is supplied as 50 ug purified immunoglobulin in 2.0 mL (25 ug/mL) ofphosphate-buffered saline (PBS). The FITC conjugate is supplied as 100 ug in 2.0 mL (50 ug/mL)of PBS. The PerCP conjugate is supplied as 50 ug in 2.0 mL (25 ug/mL) of PBS. The PerCP-Cy5.5 conjugate is supplied as 6 ug in 1.0 mL (6 ug/mL) of PBS. The APC conjugate is supplied as 12.5ug in 0.5 mL (25 ug/mL) of PBS. The APC-Cy7 conjugate is supplied as 50 ug in 0.5 mL (100 ug/mL) of PBS. PBS contains gelatin and 0.1% sodium azide. Twenty microliters (20 uL) of the monoclonal antibody or the FITC-, PerCP-, or PerCP-Cy5.5–conjugated antibody stains 106 PBMCs. Five microliters (5 uL) of the APC- or APC-Cy7–conjugated antibody stains 106 PBMCs.

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The nominal content of Silymarin is within the range 30% m/m to 65% m/m as silybin ( dry extract C25H22O10 ).

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The nominal content of silymarin is within the range 30% m/m to 65% m/m as silybin (dried extract).

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The origin of the biological additives is as follows:

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The polyclonal rabbit antisera are produced by immunization with well defined reference strains. They have been rendered specific by absorption of antibodies against other E. coli antigens.

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The potency of Heparin Sodium, calculated on the dried basis, is NLT 180 USP Heparin Units in each mg.

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The product are sterile plastic syringes which contain calcium- balanced Heparin.

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The product composed of stabilized human red cell suspended in a buffer fluid and preservatives.

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The product is a buffered bicarbonate solution in equilibrium with predetermined levels oxygen, carbon dioxide and nitrogen.\nThe mean values and the range of the analytes are specific for each lot of the product.

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The product is a human base control with addedconstituents of animal origin, chemicals and preservatives. The mean values and the range of the analytes are specific for each lot of the product.

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The product is a suspension of human blood and simulated platelets stabilized in a buffered medium.\nThis product is a stabilized liquid product manufactured under rigid quality control standards.

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The product is prepared form human serum added constituents of human and animal origins,therapeutic drugs,stabilizers and preservatives.The control is provided in lyophilized form for increased stability.

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The product is prepared form human serum with added consitituents of human and animal origins, chemicals and stabilizers. The control is provided in lyophilized form for increased stability.

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The product is prepared form human serum with added consitituents of human and animal origins, pure chemicals and stabilizers. The control is provided in lyophilized form for increased stability.

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The product is prepared form human serum with added constituents of human and animal origins.

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The product is prepared form human serum with added constituents of purified biochemicals tissue extracts of human and animal origin), chemicals, therapeutic drugs, preservative and stabilizers. The control is provided in lyophilized form for increased stability.

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The product is prepared form human serum with added drugs, constituents of human and animal origin, stabilizers and preservatives. The mean values were derived from replicate analyses and are specific for each lot of product.

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The product is prepared form human serum with added serum protein, constituents of animal origins, preservatives and stabilizers. The control is provided in liquid form for convenience.

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The product is prepared from bovine serum albumin with chemicals, stabilizers and preservatives added. The control is provided in liquid form for convenience.

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The product is prepared from human plasma, human serum and human proteins. Preservatives and stabilizers have been added to maintain product integrity.

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The product is prepared from human serum iwth added constituents of human and animal origins, preservatives and stabilizers.

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The product is prepared from human serum to which purified biochemicals (tissue extract of human and animal origin), chemicals, therapeutic drugs, preservatives and stabilizers have been added. The mean values and the range of the analytes are specific for each lot of the product.

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The product is prepared from human serum with added chemicals and constituents of human and animal origin. The control is provided in lyophilized form for increased stability.

• 關聯藥證數量: 1

The product is prepared from human serum with added consitituents of human and animal origins, pure chemicals and stabilizers. The control is provided in lyophilized form for increased stability.

• 關聯藥證數量: 1

The product is prepared from human serum with added constituents of human and animal origin, chemicals; therapeutic drugs, stabilizers and preservatives.The control is provided in liquid form.\nThe mean values and the range of the analytes are specific for each lot of the product.

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The product is prepared from human serum with added constituents of human and animal origins, chemicals and therapeutic drugs. Level 1 also contains stabilizers. The control is provided in lyophilized form.The mean values and the range of the analytes are specific for each lot of the product.

• 關聯藥證數量: 1

The product is prepared from human serum with added constituents of human and animal origins, pure chemicals and stabilizers. The control is provided in lyophilized form for increased stability.

• 關聯藥證數量: 1

The product is prepared from human serum with added constituents of purified biochemicals(tissue extract form human and animal origins), chemicals, therapeutic drugs, preservatives and stabilizers.

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The product is prepared from human urine with added constituents of human and animal origins, chemicals, preservatives and stabilizers. The mean values and the ranges of the analytes are specific for each lot of the product.

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The product is prepared from human whole blood and contains preservatives and stabilizers. The control is provided in lyophilized form for increased stability.

• 關聯藥證數量: 1

The product is prepared from human whole blood with added chemicals, and stabilizers. The control is provided in lyophilized from for increased stability.

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The product is prepared from human whole blood with pure chemicals, stabilizers added.

• 關聯藥證數量: 1

The product is prepared from human whole blood, with added chemicals, and stabilizers. The control is provided in lyophilized form for increased stability.

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The products are micro blood collection tubes without anticoagulant, the gel of SST are easy to separate.

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The products are prepared in a buffered sodium chloride diluent containing bovine albumin, glycine, and a surfactant to prevent adherence of the cell button to the test tube.

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The quality control material is prepared from human serum with nonserum constituents added. No preservatives or stabilizers were added. The constituents were adjusted to the levels listed in Expected Values.

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The quality control material is prepared from human serum with recombinant human CK-MB, human proteins, and stabilizing/bacteriostatic agents added.

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The reaction device contains a drug-protein conjugate coated membrane and a pad containing the antibody-dye conjugate in a protein matrix containing a 0.1% sodium azide.

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The reaction strip contains dye-conjugated and immobilized antibodies in a protein matrix.

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The reagent contains a near-colloidal particle activator and a chloroform extract of rabbit brain with buffer and stabilizers. Calcium Cloride:0.025 M.

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The reagent is provided in 1ml of buffered saline with 0.1% sodium azide. It contains FITC-labeled CD3, clone SK7、\nPE-labeled CD16, clone B73.1、\nCD56, clone NCAM 16.2、\nPerCP-Cy5.5-labeled CD45, clone 2D1 (HLe-1)、\nPE-Cy7-labeled CD4, clone SK3、\nAPC-labeled CD19, clone SJ25C1、\nAPC-Cy7-labeled CD8, clonenSK1.

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The reagent red cells are suspended in a preservation medium.

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The reagent red cells are suspended in a special preservation medium.\nCoombs Control Cell (Strong) are IgG sensitised Group 0 Rhesus D-positive human red cells that have been sensitised in vitro with different amounts of anti-D (IgG) antibodies.

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The reagent set is sufficient for 100 tests and consists of the following reagents :1.<5% Quinidine ANTISERUM (Mouse)in buffer containing protein as stabilizer and <0.1% sodium azide as preservative (3mL). Cap label “A”2.<0.1% Quinidine -fluorescein TRACER in buffer containing protein as stabilizer and <0.1% sodium azide as preservative (3mL). Cap label “T”3.PRE-TREATMENT BUFFER containing a surfactant and <0.1% sodium azide as preservative (3mL). Cap label “B”

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The reagent set is sufficient for 100 tests and consists of the following reagents:\n1. < 5% Digitoxin ANTISERUM (Rabbit) in buffer containing protein as stabilizer and < 0.1% sodium azide as preservative (3 mL). Cap label A\n2. < 0.1% Digitoxin-fluorescein TRACER in buffer containing protein as stabilizer, a surfactant and < 0.1% sodium azide as preservative (3 mL). Cap label T\n3. PRE-TREATMENT BUFFER containing surfactant (3 mL). Cap label B\nThe INNOFLUOR DIGITOXIN Calibrator Set consists of human serum and <0.1% sodium azide as preservative with 0, 5.0, 10.0, 20.0, 40.0, 80.0 ng/ml digitoxin:\nEach calibrator vial contains 2.5 mL, sufficient for ten dupli-cate calibration curves.

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