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] |