Felodipine
- Product NDC
- 63629-2193
- 11-digit product format
- 636292193
- Labeler code
- 63629
- Product ID
- 63629-2193_8dab6bee-ab92-4e71-96df-d5cdbba9564e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Felodipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200815
- Marketing category
- ANDA
- Marketing start
- 2009-03-31
- Substance
- FELODIPINE
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| OL961R6O2C | FELODIPINE | 72509-76-3 | FELODIPINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-2193-1 | 63629219301 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-2193-1) | 2009-03-31 | No | No | Historical |