Metronidazole
- Product NDC
- 58657-683
- 11-digit product format
- 586570683
- Labeler code
- 58657
- Product ID
- 58657-683_a989e3e7-b9d2-4dcd-8431-bb2500905247
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Method Pharmaceuticals, LLC
- Application
- ANDA070772
- Marketing category
- ANDA
- Marketing start
- 2017-09-13
- 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
FDA-Initiated Inactive NDC Indexing#