NIFEDIPINE
- Product NDC
- 68382-688
- 11-digit product format
- 683820688
- Labeler code
- 68382
- Product ID
- 68382-688_18f1ad21-11a1-4d2d-b5bc-a88ac8c02f45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NIFEDIPINE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA210184
- Marketing category
- ANDA
- Marketing start
- 2018-08-18
- 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 | 198034, 198035, 198036 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68382-688-01 | NIFEDIPINE | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | | 4 |
| 68382-688-05 | NIFEDIPINE | 500 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 500 | | 4 |
| 68382-688-10 | NIFEDIPINE | 1000 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 1000 | | 4 |
| 68382-688-16 | NIFEDIPINE | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | | 4 |
| 68382-688-77 | NIFEDIPINE | 10 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 10 | | 4 |
| 68382-688-77 | NIFEDIPINE | 10 in 1 CARTON | TABLET, EXTENDED RELEASE | 10 | | 4 |
| 68382-688-95 | NIFEDIPINE | 300 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 300 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68382-688 | NIFEDIPINE TABLET, EXTENDED RELEASE [ZYDUS PHARMACEUTICALS (USA) INC.] | 4 | Current NDC, Legacy NDC, 7 package rows | 20240118_1c857df2-9cce-40de-95c3-b1274ed1e1bc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68382-688-01 | 68382068801 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-01) | | 2018-08-18 | 0000-00-00 | No | No | Current |
| 68382-688-05 | 68382068805 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-05) | | 2018-08-18 | 0000-00-00 | No | No | Current |
| 68382-688-10 | 68382068810 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-10) | | 2018-08-18 | 0000-00-00 | No | No | Current |
| 68382-688-16 | 68382068816 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-16) | | 2018-08-18 | 0000-00-00 | No | No | Current |
| 68382-688-77 | 68382068877 | 10 BLISTER PACK in 1 CARTON (68382-688-77) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2018-08-18 | 0000-00-00 | No | No | Current |
| 68382-688-95 | 68382068895 | 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-688-95) | | 2018-08-18 | 0000-00-00 | No | No | Current |