nifedipine
- Product NDC
- 68071-4281
- 11-digit product format
- 680714281
- Labeler code
- 68071
- Product ID
- 68071-4281_bb78bbf0-c20f-398a-e053-2a95a90a7918
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nifedipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075289
- Marketing category
- ANDA
- Marketing start
- 2000-09-27
- 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
- 2022-12-31
- 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 |
|---|
| 68071-4281-3 | 68071428103 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4281-3) | 2018-02-12 | 0000-00-00 | No | No | Current |
| 68071-4281-6 | 68071428106 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4281-6) | 2018-02-12 | 0000-00-00 | No | No | Current |
| 68071-4281-9 | 68071428109 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4281-9) | 2018-02-12 | 0000-00-00 | No | No | Current |