Felodipine
- Product NDC
- 63629-2320
- 11-digit product format
- 636292320
- Labeler code
- 63629
- Product ID
- 63629-2320_f8bd8b9c-8b21-42f3-bd49-3b02b3db3e26
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Felodipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210847
- Marketing category
- ANDA
- Marketing start
- 2020-08-12
- Marketing end
- 0000-00-00
- Substance
- FELODIPINE
- Active strength
- 3 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
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2320-1 | 63629232001 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2320-1) | 2021-02-17 | 0000-00-00 | No | No | Current |