Metronidazole
- Product NDC
- 72162-2259
- 11-digit product format
- 721622259
- Labeler code
- 72162
- Product ID
- 72162-2259_23a9c9ca-e7a0-4c69-af20-621bacc1fff6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076408
- Marketing category
- ANDA
- Marketing start
- 2004-05-28
- Substance
- METRONIDAZOLE
- Active strength
- 7.5 mg/g
- 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 |
|---|
| 72162-2259-2 | 72162225902 | 45 g in 1 TUBE (72162-2259-2) | 45 g | 2024-02-23 | No | No | Historical |