Felodipine
- Product NDC
- 50090-2421
- 11-digit product format
- 500902421
- Labeler code
- 50090
- Product ID
- 50090-2421_0e0c56f0-29ee-49e1-b346-096d1ff0308d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Felodipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090365
- Marketing category
- ANDA
- Marketing start
- 2010-12-20
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 50090-2421-0 | Felodipine | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2421 | FELODIPINE TABLET, FILM COATED, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 9 | Legacy NDC, 1 package rows | 20210327_e0672664-c12a-429a-a04f-62b75fcfb0ae.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 |
|---|
| 50090-2421-0 | 50090242100 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-2421-0) | 2016-06-15 | 0000-00-00 | No | No | Current |