Nifedipine
- Product NDC
- 72162-2536
- 11-digit product format
- 721622536
- Labeler code
- 72162
- Product ID
- 72162-2536_c113fe1f-2c51-4db8-8efe-1a295c79823b
- 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
- 90 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 |
|---|
| 72162-2536-1 | 72162253601 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2536-1) | 2025-09-19 | No | No | Historical |