Nifedipine
- Product NDC
- 55154-5363
- 11-digit product format
- 551545363
- Labeler code
- 55154
- Product ID
- 55154-5363_79046dde-2a61-4a15-8ebb-1dfee4123507
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nifedipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA090649
- Marketing category
- ANDA
- Marketing start
- 2010-06-23
- Marketing end
- 0000-00-00
- Substance
- NIFEDIPINE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record