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Metronidazole
Metronidazole - 63629-1386-1 - (Metronidazole)
Drug Information of Metronidazole
| Product NDC: | 63629-1386 |
| Proprietary Name: | Metronidazole |
| Non Proprietary Name: | Metronidazole |
| Active Ingredient(s): | 500 mg/1 & nbsp; Metronidazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metronidazole
| Product NDC: | 63629-1386 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070033 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100901 |
Package Information of Metronidazole
| Package NDC: | 63629-1386-1 |
| Package Description: | 20 TABLET in 1 BOTTLE (63629-1386-1) |
NDC Information of Metronidazole
| NDC Code | 63629-1386-1 |
| Proprietary Name | Metronidazole |
| Package Description | 20 TABLET in 1 BOTTLE (63629-1386-1) |
| Product NDC | 63629-1386 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metronidazole |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | ANDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | METRONIDAZOLE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |
