Felodipine
- Product NDC
- 50090-5870
- 11-digit product format
- 500905870
- Labeler code
- 50090
- Product ID
- 50090-5870_4c349c25-c277-4c0f-9ca4-f5296b652eff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Felodipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203417
- Marketing category
- ANDA
- Marketing start
- 2013-01-17
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5870-0 | Felodipine | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5870 | FELODIPINE TABLET, FILM COATED, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 5 | Current NDC, Legacy NDC, 1 package rows | 20231125_be3bc927-1ba5-4cdd-9986-64ff29789d7e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5870-0 | 50090587000 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5870-0) | 2021-12-09 | 0000-00-00 | No | No | Current |