metronidazole
- Product NDC
- 71335-2949
- 11-digit product format
- 713352949
- Labeler code
- 71335
- Product ID
- 71335-2949_c10ff458-16a6-496f-b999-614d87fc48ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070772
- Marketing category
- ANDA
- Marketing start
- 2025-01-04
- Substance
- METRONIDAZOLE
- Active strength
- 125 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 140QMO216E | METRONIDAZOLE | 443-48-1 | METRONIDAZOLE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2949-1 | 71335294901 | 56 TABLET in 1 BOTTLE (71335-2949-1) | 56 tablet | 2025-10-30 | No | No | Historical |