FDA.reportPublic FDA data

Felodipine

Product NDC
68071-4466
11-digit product format
680714466
Labeler code
68071
Product ID
68071-4466_6e5fd2b9-74dc-021f-e053-2a91aa0a87eb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Felodipine
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA075896
Marketing category
ANDA
Marketing start
2004-11-02
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
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-4466-82020-06-15C16284748780-19d75b9d0-5275-f424-e053-dadaa90a57ce6e5fd2b9-74db-021f-e053-2a91aa0a87eb
68071-4466-92020-06-15C16284748780-19d75b9d0-5275-f424-e053-dadaa90a57ce6e5fd2b9-74db-021f-e053-2a91aa0a87eb
68071-4466-82020-01-31C16284748780-19d75b9d0-5275-f424-e053-dadaa90a57ce6e5fd2b9-74db-021f-e053-2a91aa0a87eb
68071-4466-92020-01-31C16284748780-19d75b9d0-5275-f424-e053-dadaa90a57ce6e5fd2b9-74db-021f-e053-2a91aa0a87eb