Nifedipine
- Product NDC
- 60760-859
- 11-digit product format
- 607600859
- Labeler code
- 60760
- Product ID
- 60760-859_43ce1c3b-6ed0-7d02-e063-6294a90ab371
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA210614
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| I9ZF7L6G2L | NIFEDIPINE | 21829-25-4 | NIFEDIPINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-859-90 | 60760085990 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-859-90) | 2024-06-01 | No | No | Historical |