Metronidazole
- Product NDC
- 68788-6843
- 11-digit product format
- 687886843
- Labeler code
- 68788
- Product ID
- 68788-6843_c6c8fbf6-7ef2-453b-bce2-3ffcfad960ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA205245
- Marketing category
- ANDA
- Marketing start
- 2016-12-06
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6843-1 | 68788684301 | 14 TABLET in 1 BOTTLE (68788-6843-1) | 14 tablet | 2016-12-06 | 0000-00-00 | No | No | Current |
| 68788-6843-2 | 68788684302 | 21 TABLET in 1 BOTTLE (68788-6843-2) | 21 tablet | 2016-12-06 | 0000-00-00 | No | No | Current |
| 68788-6843-3 | 68788684303 | 30 TABLET in 1 BOTTLE (68788-6843-3) | 30 tablet | 2016-12-06 | 0000-00-00 | No | No | Current |
| 68788-6843-4 | 68788684304 | 28 TABLET in 1 BOTTLE (68788-6843-4) | 28 tablet | 2016-12-06 | 0000-00-00 | No | No | Current |
| 68788-6843-7 | 68788684307 | 42 TABLET in 1 BOTTLE (68788-6843-7) | 42 tablet | 2016-12-06 | 0000-00-00 | No | No | Current |