Metronidazole
- Product NDC
- 68788-8230
- 11-digit product format
- 687888230
- Labeler code
- 68788
- Product ID
- 68788-8230_feec1c25-ead5-4a11-beb1-ca1e67737a46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA203974
- Marketing category
- ANDA
- Marketing start
- 2022-08-08
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8230-2 | 68788823002 | 21 TABLET in 1 BOTTLE (68788-8230-2) | 21 tablet | 2022-08-08 | 0000-00-00 | No | No | Current |