| Product NDC: | 0025-1961 |
| Proprietary Name: | Flagyl ER |
| Non Proprietary Name: | Metronidazole |
| Active Ingredient(s): | 750 mg/1 & nbsp; Metronidazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0025-1961 |
| Labeler Name: | G.D. Searle LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020868 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19971126 |
| Package NDC: | 0025-1961-30 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0025-1961-30) |
| NDC Code | 0025-1961-30 |
| Proprietary Name | Flagyl ER |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0025-1961-30) |
| Product NDC | 0025-1961 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metronidazole |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19971126 |
| Marketing Category Name | NDA |
| Labeler Name | G.D. Searle LLC |
| Substance Name | METRONIDAZOLE |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |