Felodipine
- Product NDC
- 0615-6573
- 11-digit product format
- 006156573
- Labeler code
- 0615
- Product ID
- 0615-6573_1b5decaf-f1c9-44b7-9b2d-de3fc5b7cc99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Felodipine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA078855
- Marketing category
- ANDA
- Marketing start
- 2009-11-16
- 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
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#