Metronidazole
- Product NDC
- 50090-5691
- 11-digit product format
- 500905691
- Labeler code
- 50090
- Product ID
- 50090-5691_92d7f3e6-cbfc-49e1-937f-1968c988c21d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203974
- Marketing category
- ANDA
- Marketing start
- 2015-05-29
- Substance
- METRONIDAZOLE
- Active strength
- 250 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 |
|---|
| 50090-5691-0 | 50090569100 | 21 TABLET in 1 BOTTLE (50090-5691-0) | 21 tablet | 2021-09-21 | No | No | Historical |
| 50090-5691-1 | 50090569101 | 28 TABLET in 1 BOTTLE (50090-5691-1) | 28 tablet | 2021-09-21 | No | No | Historical |
| 50090-5691-2 | 50090569102 | 30 TABLET in 1 BOTTLE (50090-5691-2) | 30 tablet | 2021-09-21 | No | No | Historical |