Felodipine
- Product NDC
- 72162-1744
- 11-digit product format
- 721621744
- Labeler code
- 72162
- Product ID
- 72162-1744_323f2005-568b-42e4-ae0e-b4a26167b32f
- 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
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Felodipine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FELODIPINE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | OL961R6O2C |
| Rxcui | 402695 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1744-5 | Felodipine | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 102 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1744 | FELODIPINE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 102 | Current NDC, 1 package rows | 20250403_2daac7f7-66a8-4be7-b7de-4f1e60bb21f9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1744-5 | 72162174405 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-1744-5) | 2024-02-02 | No | No | Historical |