Nifedipine
- Product NDC
- 50436-4068
- 11-digit product format
- 504364068
- Labeler code
- 50436
- Product ID
- 50436-4068_1ff669f1-8947-4022-8c55-a889b8a6c7e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077127
- Marketing category
- ANDA
- Marketing start
- 2005-11-21
- Marketing end
- 0000-00-00
- Substance
- NIFEDIPINE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record