Metronidazole
- Product NDC
- 68788-9082
- 11-digit product format
- 687889082
- Labeler code
- 68788
- Product ID
- 68788-9082_2412148b-ccde-4c5d-8e7f-b5c4488d8f5a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA070027
- Marketing category
- ANDA
- Marketing start
- 2010-09-01
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record