Felodipine
- Product NDC
- 71335-2175
- 11-digit product format
- 713352175
- Labeler code
- 71335
- Product ID
- 71335-2175_cea3457b-ddba-4364-ae9d-141261c6c2de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Felodipine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204800
- Marketing category
- ANDA
- Marketing start
- 2020-10-12
- Substance
- FELODIPINE
- Active strength
- 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 |
|---|
| 71335-2175-1 | 71335217501 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2175-1) | 2022-10-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Felodipine Tablets USP | Bryant Ranch Prepack | 2025-03-31 | HUMAN PRESCRIPTION DRUG LABEL | 103 |