Felodipine
- Product NDC
- 68151-3084
- 11-digit product format
- 681513084
- Labeler code
- 68151
- Product ID
- 68151-3084_98d681ac-3b67-4979-ae0d-5b81e9c512a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Felodipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA090365
- Marketing category
- ANDA
- Marketing start
- 2010-12-20
- Marketing end
- 0000-00-00
- Substance
- FELODIPINE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-3084-8 | Felodipine | 1 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-3084 | FELODIPINE TABLET, FILM COATED, EXTENDED RELEASE [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20171228_103d9fb6-8433-4386-9f2e-d07f4c560aea.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-3084-8 | 68151308408 | 1 in 1 BOTTLE | Historical |