Metronidazole
- Product NDC
- 70934-970
- 11-digit product format
- 709340970
- Labeler code
- 70934
- Product ID
- 70934-970_e0033fd0-1b07-0671-e053-2a95a90a1292
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METRONIDAZOLE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA205245
- Marketing category
- ANDA
- Marketing start
- 2022-05-26
- Marketing end
- 0000-00-00
- Substance
- METRONIDAZOLE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-970-14 | 70934097014 | 14 TABLET in 1 BOTTLE, PLASTIC (70934-970-14) | 14 tablet | 2022-05-26 | 0000-00-00 | No | No | Current |