Nifedipine
- Product NDC
- 0904-6545
- 11-digit product format
- 009046545
- Labeler code
- 0904
- Product ID
- 0904-6545_ee37b27f-0477-4fe1-bd82-4bd4cafbbaf6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA077899
- Marketing category
- ANDA
- Marketing start
- 2007-06-22
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record