Nifedipine
- Product NDC
- 62112-8045
- 11-digit product format
- 621128045
- Labeler code
- 62112
- Product ID
- 62112-8045_902e6043-5b3d-9a4b-e053-2a95a90a3d66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Intergel Pharmaceuticals Inc
- Application
- ANDA072781
- Marketing category
- ANDA
- Marketing start
- 2009-08-01
- Marketing end
- 0000-00-00
- Substance
- NIFEDIPINE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 62112-8045-2 | Nifedipine | 100 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 100 | | 7 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62112-8045 | NIFEDIPINE CAPSULE, LIQUID FILLED [INTERGEL PHARMACEUTICALS INC] | 7 | Legacy NDC, 1 package rows | 20190816_a3daa0fc-7ec3-42c2-91b2-8418331dd0fc.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 |
|---|
| 62112-8045-2 | 62112804502 | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (62112-8045-2) | 2009-08-01 | 0000-00-00 | No | No | Current |