Metronidazole 61919-0032
Product NDC
61919-0032- Manufacturer
- Direct_rx
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 21, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA203458
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Metronidazole | 500 mg/1 |
Drug Class
Nitroimidazole Antimicrobial [EPC]Nitroimidazole Antimicrobial [EPC]Nitroimidazoles [CS]
Packaging Options(1)
10 TABLET, FILM COATED in 1 BOTTLE (61919-032-10)