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Flagyl
Flagyl - 0025-1821-31 - (Metronidazole)
Drug Information of Flagyl
| Product NDC: | 0025-1821 |
| Proprietary Name: | Flagyl |
| Non Proprietary Name: | Metronidazole |
| Active Ingredient(s): | 500 mg/1 & nbsp; Metronidazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flagyl
| Product NDC: | 0025-1821 |
| Labeler Name: | G.D. Searle LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012623 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19630718 |
Package Information of Flagyl
| Package NDC: | 0025-1821-31 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0025-1821-31) |
NDC Information of Flagyl
| NDC Code | 0025-1821-31 |
| Proprietary Name | Flagyl |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0025-1821-31) |
| Product NDC | 0025-1821 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metronidazole |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19630718 |
| Marketing Category Name | NDA |
| Labeler Name | G.D. Searle LLC |
| Substance Name | METRONIDAZOLE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |
