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Meropenem
Meropenem - 63323-507-21 - (Meropenem)
Drug Information of Meropenem
| Product NDC: | 63323-507 |
| Proprietary Name: | Meropenem |
| Non Proprietary Name: | Meropenem |
| Active Ingredient(s): | 500 mg/10mL & nbsp; Meropenem |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Meropenem
| Product NDC: | 63323-507 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091404 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111014 |
Package Information of Meropenem
| Package NDC: | 63323-507-21 |
| Package Description: | 10 VIAL in 1 CARTON (63323-507-21) > 10 mL in 1 VIAL |
NDC Information of Meropenem
| NDC Code | 63323-507-21 |
| Proprietary Name | Meropenem |
| Package Description | 10 VIAL in 1 CARTON (63323-507-21) > 10 mL in 1 VIAL |
| Product NDC | 63323-507 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Meropenem |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111014 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | MEROPENEM |
| Strength Number | 500 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Carbapenems [Chemical/Ingredient],Penem Antibacterial [EPC] |
