Nifedipine
- Product NDC
- 72162-2535
- 11-digit product format
- 721622535
- Labeler code
- 72162
- Product ID
- 72162-2535_9205be3f-c95c-4653-83a8-92ddd6398523
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213361
- Marketing category
- ANDA
- Marketing start
- 2021-07-19
- 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 |
|---|
| 72162-2535-1 | 72162253501 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2535-1) | 2025-09-19 | No | No | Historical |