nifedipine
- Product NDC
- 72214-503
- 11-digit product format
- 722140503
- Labeler code
- 72214
- Product ID
- 72214-503_279aef53-239a-403d-82d3-01387ee3580e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nifedipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Elite pharmaceutical Technology (Shanghai) Co., Ltd
- Application
- ANDA212016
- Marketing category
- ANDA
- Marketing start
- 2021-01-01
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72214-503-12 | nifedipine | 100 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 100 | | 2 |
| 72214-503-13 | nifedipine | 300 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 300 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72214-503 | NIFEDIPINE TABLET, FILM COATED, EXTENDED RELEASE [ELITE PHARMACEUTICAL TECHNOLOGY (SHANGHAI) CO., LTD] | 2 | Legacy NDC, 2 package rows | 20210112_1c027c28-4000-4c4c-b4a1-4cc89412db77.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 |
|---|
| 72214-503-12 | 72214050312 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72214-503-12) | 2021-01-01 | 0000-00-00 | No | No | Current |
| 72214-503-13 | 72214050313 | 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72214-503-13) | 2021-01-01 | 0000-00-00 | No | No | Current |