Nifedipine
- Product NDC
- 55154-8199
- 11-digit product format
- 551548199
- Labeler code
- 55154
- Product ID
- 55154-8199_3f7d2eeb-9f3e-4774-a6af-86b03ff5ac13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA072781
- Marketing category
- ANDA
- Marketing start
- 2019-06-01
- 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
- 2022-12-31
- 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 |
|---|
| 55154-8199-0 | 55154819900 | 10 BLISTER PACK in 1 BAG (55154-8199-0) > 1 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2019-06-01 | 0000-00-00 | No | No | Current |