UNASYN - 0049-0031-83 - (AMPICILLIN SODIUM and SULBACTAM SODIUM)

Alphabetical Index


Drug Information of UNASYN

Product NDC: 0049-0031
Proprietary Name: UNASYN
Non Proprietary Name: AMPICILLIN SODIUM and SULBACTAM SODIUM
Active Ingredient(s): 1; .5    g/1; g/1 & nbsp;   AMPICILLIN SODIUM and SULBACTAM SODIUM
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of UNASYN

Product NDC: 0049-0031
Labeler Name: Roerig
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA062901
Marketing Category: NDA
Start Marketing Date: 19911122

Package Information of UNASYN

Package NDC: 0049-0031-83
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (0049-0031-83) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE

NDC Information of UNASYN

NDC Code 0049-0031-83
Proprietary Name UNASYN
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (0049-0031-83) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Product NDC 0049-0031
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMPICILLIN SODIUM and SULBACTAM SODIUM
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19911122
Marketing Category Name NDA
Labeler Name Roerig
Substance Name AMPICILLIN SODIUM; SULBACTAM SODIUM
Strength Number 1; .5
Strength Unit g/1; g/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitors [MoA],beta Lactamase Inhibitor [EPC]

Complete Information of UNASYN


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