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Ampicillin and Sulbactam
Ampicillin and Sulbactam - 55150-118-99 - (Ampicillin Sodium and Sulbactam Sodium)
Drug Information of Ampicillin and Sulbactam
| Product NDC: | 55150-118 |
| Proprietary Name: | Ampicillin and Sulbactam |
| Non Proprietary Name: | Ampicillin Sodium and Sulbactam Sodium |
| Active Ingredient(s): | 100; 50 mg/mL; mg/mL & nbsp; Ampicillin Sodium and Sulbactam Sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ampicillin and Sulbactam
| Product NDC: | 55150-118 |
| Labeler Name: | AuroMedics Pharma LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090339 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120210 |
Package Information of Ampicillin and Sulbactam
| Package NDC: | 55150-118-99 |
| Package Description: | 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-118-99) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
NDC Information of Ampicillin and Sulbactam
| NDC Code | 55150-118-99 |
| Proprietary Name | Ampicillin and Sulbactam |
| Package Description | 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-118-99) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
| Product NDC | 55150-118 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ampicillin Sodium and Sulbactam Sodium |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120210 |
| Marketing Category Name | ANDA |
| Labeler Name | AuroMedics Pharma LLC |
| Substance Name | AMPICILLIN SODIUM; SULBACTAM SODIUM |
| Strength Number | 100; 50 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitors [MoA],beta Lactamase Inhibitor [EPC] |
