nifedipine
- Product NDC
- 59762-1004
- 11-digit product format
- 597621004
- Labeler code
- 59762
- Product ID
- 59762-1004_6781ba59-f21a-4c40-a4bc-7abe0061ec91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nifedipine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA018482
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-03-25
- Marketing end
- 0000-00-00
- Substance
- NIFEDIPINE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59762-1004-1 | 59762100401 | 100 CAPSULE in 1 BOTTLE (59762-1004-1) | 100 capsule | 2013-03-25 | 0000-00-00 | No | No | Current |