Felopdipine
- Product NDC
- 50090-7206
- 11-digit product format
- 500907206
- Labeler code
- 50090
- Product ID
- 50090-7206_3e6e1e52-669c-49d7-a682-840308927b98
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Felodipine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA210847
- Marketing category
- ANDA
- Marketing start
- 2023-03-31
- Substance
- FELODIPINE
- 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
- 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 |
|---|
| 50090-7206-0 | 50090720600 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7206-0) | 2024-08-05 | No | No | Historical |