Felodipine

Product NDC
59746-370
11-digit product format
597460370
Labeler code
59746
Product ID
59746-370_65e89353-178f-49db-ae9c-998d58fa58a4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Felodipine
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Jubilant Cadista Pharmaceuticals Inc.
Application
ANDA203983
Marketing category
ANDA
Marketing start
2016-08-19
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
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59746-370-01EA - Each59746-370fc6943a4-a217-44fb-97b1-20cc42685a7812018-02-20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
59746-370-0159746037001100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59746-370-01) 2016-08-190000-00-00NoNoCurrent
59746-370-0559746037005500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59746-370-05) 2016-08-190000-00-00NoNoCurrent
59746-370-10597460370101000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59746-370-10) 2016-08-190000-00-00NoNoCurrent
59746-370-305974603703030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59746-370-30) 2016-08-190000-00-00NoNoCurrent
59746-370-905974603709090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59746-370-90) 2016-08-190000-00-00NoNoCurrent