Metronidazole
- Product NDC
- 70518-3073
- 11-digit product format
- 705183073
- Labeler code
- 70518
- Product ID
- 70518-3073_e5ba2c59-93e8-3c1f-e053-2995a90a3bd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METRONIDAZOLE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205245
- Marketing category
- ANDA
- Marketing start
- 2021-04-19
- Marketing end
- 0000-00-00
- Substance
- METRONIDAZOLE
- Active strength
- 250 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 |
|---|
| 70518-3073-0 | 70518307300 | 30 TABLET in 1 BLISTER PACK (70518-3073-0) | 30 tablet | 2021-04-19 | 0000-00-00 | No | No | Current |
| 70518-3073-1 | 70518307301 | 28 TABLET in 1 BLISTER PACK (70518-3073-1) | 28 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |
| 70518-3073-2 | 70518307302 | 28 TABLET in 1 BLISTER PACK (70518-3073-2) | 28 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |
| 70518-3073-3 | 70518307303 | 28 TABLET in 1 BLISTER PACK (70518-3073-3) | 28 tablet | 2022-08-07 | 0000-00-00 | No | No | Current |