Nifedipine
- Product NDC
- 60687-425
- 11-digit product format
- 606870425
- Labeler code
- 60687
- Product ID
- 60687-425_c47e359d-6010-5e3b-e053-2995a90ae1d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA072781
- Marketing category
- ANDA
- Marketing start
- 2019-06-01
- Marketing end
- 2022-05-31
- 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
- 0000-00-00
- 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 |
|---|
| 60687-425-01 | 60687042501 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-425-01) > 1 CAPSULE in 1 BLISTER PACK (60687-425-11) | 100 blister pack | 2019-06-01 | 0000-00-00 | No | No | Current |