Nifedipine
- Product NDC
- 67296-2157
- 11-digit product format
- 672962157
- Labeler code
- 67296
- Product ID
- 67296-2157_45d26939-fe46-b92b-e063-6294a90a64bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA216067
- Marketing category
- ANDA
- Marketing start
- 2022-03-30
- Substance
- NIFEDIPINE
- Active strength
- 30 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nifedipine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NIFEDIPINE | 30 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I9ZF7L6G2L |
| Rxcui | 1812011 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-2157-1 | Nifedipine | 10 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 10 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-2157 | NIFEDIPINE TABLET, EXTENDED RELEASE [REDPHARM DRUG] | 1 | Current NDC, 1 package rows | 20250410_32526983-f53a-fa68-e063-6394a90aa13f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2157-1 | 67296215701 | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2157-1) | 2022-03-30 | No | No | Current |