| Product NDC: | 63323-508 |
| Proprietary Name: | Meropenem |
| Non Proprietary Name: | Meropenem |
| Active Ingredient(s): | 1 g/20mL & nbsp; Meropenem |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63323-508 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091404 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111026 |
| Package NDC: | 63323-508-30 |
| Package Description: | 10 VIAL in 1 CARTON (63323-508-30) > 20 mL in 1 VIAL |
| NDC Code | 63323-508-30 |
| Proprietary Name | Meropenem |
| Package Description | 10 VIAL in 1 CARTON (63323-508-30) > 20 mL in 1 VIAL |
| Product NDC | 63323-508 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Meropenem |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111026 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | MEROPENEM |
| Strength Number | 1 |
| Strength Unit | g/20mL |
| Pharmaceutical Classes | Carbapenems [Chemical/Ingredient],Penem Antibacterial [EPC] |