Nifedipine
- Product NDC
- 50090-5328
- 11-digit product format
- 500905328
- Labeler code
- 50090
- Product ID
- 50090-5328_6ccf2e72-eb18-47e2-8d27-f7fe64895778
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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 |
|---|
| 50090-5328-0 | 50090532800 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5328-0) | 2020-11-02 | 0000-00-00 | No | No | Current |
| 50090-5328-1 | 50090532801 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5328-1) | 2020-11-02 | 0000-00-00 | No | No | Current |
| 50090-5328-2 | 50090532802 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5328-2) | 2020-11-02 | 0000-00-00 | No | No | Current |