Nifedipine
- Product NDC
- 42192-615
- 11-digit product format
- 421920615
- Labeler code
- 42192
- Product ID
- 42192-615_e1535dde-a32a-4a95-b1d7-2b7f8a874dee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nifedipine
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Acella Pharmaceuticals, LLC
- Application
- ANDA072781
- Marketing category
- ANDA
- Marketing start
- 2009-08-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42192-615-01 | 42192061501 | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (42192-615-01) | 2009-08-01 | 0000-00-00 | No | No | Current |