01 1ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE; RIBOFLAVIN 5-PHOSPHATE SODIUM; THIAMINE; VITAMIN A; VITAMIN E
02 2CEFOTETAN DISODIUM
03 1DOBUTAMINE HYDROCHLORIDE
04 1DOPAMINE HYDROCHLORIDE
05 1FLURANDRENOLIDE
01 6TELIGENT
01 5INJECTABLE;INJECTION
02 1OINTMENT;TOPICAL
01 10.05%
02 1100MG/VIAL;0.06MG/VIAL;0.005MG/VIAL;15MG/VIAL;5MCG/VIAL;0.4MG/VIAL;40MG/VIAL;4MG/VIAL;3.6MG/VIAL;3MG/VIAL;1MG/VIAL;10MG/VIAL
03 140MG/ML
04 1EQ 12.5MG BASE/ML
05 1EQ 1GM BASE/VIAL
06 1EQ 2GM BASE/VIAL
01 6USA
Regulatory Info : DISCN
Registration Country : USA
ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE; RIBOFLAVIN 5-PHOSPHATE SODIUM; THIAMINE; VITAMIN A; VITAMIN E
Dosage Form : INJECTABLE;INJECTION
Brand Name : M.V.I.-12 LYOPHILIZED
Dosage Strength : 100MG/VIAL;0.06MG/VIAL...
Packaging :
Approval Date : 1985-08-08
Application Number : 18933
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CEFOTAN
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 1993-04-29
Application Number : 63293
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CEFOTAN
Dosage Strength : EQ 2GM BASE/VIAL
Packaging :
Approval Date : 1993-04-29
Application Number : 63293
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : DOBUTAMINE HYDROCHLORIDE
Dosage Strength : EQ 12.5MG BASE/ML
Packaging :
Approval Date : 1995-02-21
Application Number : 74098
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : DOPAMINE HYDROCHLORIDE
Dosage Strength : 40MG/ML
Packaging :
Approval Date : 1983-06-28
Application Number : 18656
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : OINTMENT;TOPICAL
Brand Name : FLURANDRENOLIDE
Dosage Strength : 0.05%
Packaging :
Approval Date : 2016-12-30
Application Number : 207851
Regulatory Info : RX
Registration Country : USA
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