Nifedipine
- Product NDC
- 10370-678
- 11-digit product format
- 103700678
- Labeler code
- 10370
- Product ID
- 10370-678_4d6be233-5b05-4efe-88ff-370ca1be90e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA077899
- Marketing category
- ANDA
- Marketing start
- 2016-03-02
- Marketing end
- 2019-11-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record