| Product NDC: | 0069-2390 |
| Proprietary Name: | Metronidazole |
| Non Proprietary Name: | Metronidazole |
| Active Ingredient(s): | 500 mg/100mL & nbsp; Metronidazole |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0069-2390 |
| Labeler Name: | Pfizer Labs, Division of Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078084 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081120 |
| Package NDC: | 0069-2390-01 |
| Package Description: | 24 BAG in 1 CARTON (0069-2390-01) > 100 mL in 1 BAG |
| NDC Code | 0069-2390-01 |
| Proprietary Name | Metronidazole |
| Package Description | 24 BAG in 1 CARTON (0069-2390-01) > 100 mL in 1 BAG |
| Product NDC | 0069-2390 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metronidazole |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20081120 |
| Marketing Category Name | ANDA |
| Labeler Name | Pfizer Labs, Division of Pfizer Inc |
| Substance Name | METRONIDAZOLE |
| Strength Number | 500 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |