metronidazole
- Product NDC
- 68382-850
- 11-digit product format
- 683820850
- Labeler code
- 68382
- Product ID
- 68382-850_4d54fa70-356a-4111-b909-61475e772c03
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA206560
- Marketing category
- ANDA
- Marketing start
- 2017-01-19
- Marketing end
- 2019-11-30
- Substance
- METRONIDAZOLE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record