Nifedipine
- Product NDC
- 68788-6971
- 11-digit product format
- 687886971
- Labeler code
- 68788
- Product ID
- 68788-6971_c9dcece8-30b0-4924-a0a7-7484392347e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA203126
- Marketing category
- ANDA
- Marketing start
- 2017-05-22
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6971-1 | 68788697101 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6971-1) | 2017-05-22 | 0000-00-00 | No | No | Current |
| 68788-6971-3 | 68788697103 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6971-3) | 2017-05-22 | 0000-00-00 | No | No | Current |
| 68788-6971-6 | 68788697106 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6971-6) | 2017-05-22 | 0000-00-00 | No | No | Current |
| 68788-6971-9 | 68788697109 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6971-9) | 2017-05-22 | 0000-00-00 | No | No | Current |