Nifedipine
- Product NDC
- 50268-601
- 11-digit product format
- 502680601
- Labeler code
- 50268
- Product ID
- 50268-601_ed859c86-eb82-9053-e053-2a95a90a6e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA072556
- Marketing category
- ANDA
- Marketing start
- 2015-07-29
- Marketing end
- 0000-00-00
- Substance
- NIFEDIPINE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50268-601-15 | 50268060115 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-601-15) > 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (50268-601-11) | 50 blister pack | 2015-07-29 | 0000-00-00 | No | No | Current |