Metronidazole
- Product NDC
- 68788-7739
- 11-digit product format
- 687887739
- Labeler code
- 68788
- Product ID
- 68788-7739_bb1bdc62-9db5-413d-9605-f35a402d7ec4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METRONIDAZOLE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA205245
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7739-1 | 68788773901 | 14 TABLET in 1 BOTTLE, PLASTIC (68788-7739-1) | 14 tablet | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7739-2 | 68788773902 | 21 TABLET in 1 BOTTLE, PLASTIC (68788-7739-2) | 21 tablet | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7739-3 | 68788773903 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-7739-3) | 30 tablet | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7739-4 | 68788773904 | 28 TABLET in 1 BOTTLE, PLASTIC (68788-7739-4) | 28 tablet | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7739-6 | 68788773906 | 60 TABLET in 1 BOTTLE, PLASTIC (68788-7739-6) | 60 tablet | 2020-07-01 | 0000-00-00 | No | No | Current |