Nifedipine
- Product NDC
- 68788-6773
- 11-digit product format
- 687886773
- Labeler code
- 68788
- Product ID
- 68788-6773_3146d8f0-2443-4ee8-ad8f-e561d0915924
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA203126
- Marketing category
- ANDA
- Marketing start
- 2016-10-24
- 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