Nifedipine
- Product NDC
- 59651-296
- 11-digit product format
- 596510296
- Labeler code
- 59651
- Product ID
- 59651-296_4d72a04e-43a6-4fa4-bd1c-1360c4539d71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nifedipine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NIFEDIPINE | 60 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I9ZF7L6G2L |
| Rxcui | 198034, 198035, 198036 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59651-296-01 | Nifedipine | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59651-296 | NIFEDIPINE TABLET, EXTENDED RELEASE [AUROBINDO PHARMA LIMITED] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250101_eb70b7ff-f9f0-41d0-901a-f4c04ae9ed46.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59651-296-01 | 59651029601 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-296-01) | 2021-07-19 | 0000-00-00 | No | No | Current |