Nifedipine
- Product NDC
- 60429-163
- 11-digit product format
- 604290163
- Labeler code
- 60429
- Product ID
- 60429-163_92753abd-3f1a-8681-e053-2a95a90a1819
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA072781
- Marketing category
- ANDA
- Marketing start
- 1993-07-30
- 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 |
|---|
| 60429-163-01 | 60429016301 | 100 CAPSULE in 1 BOTTLE (60429-163-01) | 100 capsule | 2017-08-01 | 0000-00-00 | No | No | Current |