Metronidazole
- Product NDC
- 72162-2403
- 11-digit product format
- 721622403
- Labeler code
- 72162
- Product ID
- 72162-2403_9e05f3f2-a880-4e10-af96-479bba15d947
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203458
- Marketing category
- ANDA
- Marketing start
- 2014-06-01
- Substance
- METRONIDAZOLE
- Active strength
- 500 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2403-2 | 72162240302 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2403-2) | 2024-10-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metronidazole Tablets USP | Bryant Ranch Prepack | 2024-10-08 | HUMAN PRESCRIPTION DRUG LABEL | 100 |