Metronidazole
- Product NDC
- 63187-711
- 11-digit product format
- 631870711
- Labeler code
- 63187
- Product ID
- 63187-711_05b4ca16-22f5-40db-9887-ad6b07c8f99d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA079067
- Marketing category
- ANDA
- Marketing start
- 2013-12-16
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record