Nifedipine
- Product NDC
- 70934-577
- 11-digit product format
- 709340577
- Labeler code
- 70934
- Product ID
- 70934-577_abfb8bbf-a5c0-119f-e053-2995a90a0590
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA203126
- Marketing category
- ANDA
- Marketing start
- 2020-02-25
- Marketing end
- 0000-00-00
- Substance
- NIFEDIPINE
- Active strength
- 90 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
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 |
|---|
| 70934-577-30 | 70934057730 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-577-30) | 2020-02-25 | 0000-00-00 | No | No | Current |