Metronidazole
- Product NDC
- 68788-9397
- 11-digit product format
- 687889397
- Labeler code
- 68788
- Product ID
- 68788-9397_48d2d9b7-05e2-44b5-b6a5-056eb28025ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metronidazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record