Nifedipine
- Product NDC
- 68071-4411
- 11-digit product format
- 680714411
- Labeler code
- 68071
- Product ID
- 68071-4411_d7750461-1213-6fb1-e053-2a95a90a12d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA202987
- Marketing category
- ANDA
- Marketing start
- 2017-02-15
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4411-3 | 68071441103 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4411-3) | 2018-04-30 | 0000-00-00 | No | No | Current |
| 68071-4411-6 | 68071441106 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4411-6) | 2018-04-30 | 0000-00-00 | No | No | Current |
| 68071-4411-9 | 68071441109 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4411-9) | 2018-04-30 | 0000-00-00 | No | No | Current |