Felodipine
- Product NDC
- 71335-1486
- 11-digit product format
- 713351486
- Labeler code
- 71335
- Product ID
- 71335-1486_4752a2b5-f4a9-4f0f-b9c9-6d97109f6a15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Felodipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090365
- Marketing category
- ANDA
- Marketing start
- 2010-12-20
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Felodipine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FELODIPINE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | OL961R6O2C |
| Rxcui | 402696 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1486-1 | 71335148601 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1486-1) | 2020-01-21 | 0000-00-00 | No | No | Current |