Nifedipine
- Product NDC
- 50090-4442
- 11-digit product format
- 500904442
- Labeler code
- 50090
- Product ID
- 50090-4442_5a35a8bd-e38b-47df-8a25-513aebeb0cec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 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 |
|---|
| 50090-4442-0 | 50090444200 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4442-0) | 2019-07-26 | 0000-00-00 | No | No | Current |
| 50090-4442-2 | 50090444202 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4442-2) | 2019-07-26 | 0000-00-00 | No | No | Current |