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