NIFEdipine
- Product NDC
- 68071-3281
- 11-digit product format
- 680713281
- Labeler code
- 68071
- Product ID
- 68071-3281_bb1723c5-7163-d227-e053-2995a90a35e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NIFEdipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA203126
- Marketing category
- ANDA
- Marketing start
- 2014-11-01
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 68071-3281-3 | 68071328103 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3281-3) | 2017-05-23 | 0000-00-00 | No | No | Current |
| 68071-3281-5 | 68071328105 | 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3281-5) | 2017-05-23 | 0000-00-00 | No | No | Current |
| 68071-3281-6 | 68071328106 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3281-6) | 2017-05-23 | 0000-00-00 | No | No | Current |
| 68071-3281-9 | 68071328109 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3281-9) | 2017-05-23 | 0000-00-00 | No | No | Current |