Carvedilol

Product NDC
50090-1856
11-digit product format
500901856
Labeler code
50090
Product ID
50090-1856_93896706-1b3e-4c2b-8c97-affd6759d016
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carvedilol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078332
Marketing category
ANDA
Marketing start
2007-09-05
Marketing end
0000-00-00
Substance
CARVEDILOL
Active strength
3 mg/1
Pharmacologic classes
Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-1856-0EA - Each50090-18564d0fc93d-3e5c-447f-a87a-da5c5a35a76f12021-09-07
50090-1856-1EA - Each50090-185639d4d10b-b2e6-426c-b915-05f99bf4e9a012021-09-07
50090-1856-3EA - Each50090-1856fd955d0d-3d27-4aee-874e-fd598790cd5e12021-09-07

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-1856-05009018560060 TABLET, FILM COATED in 1 BOTTLE (50090-1856-0) 2015-06-020000-00-00NoNoCurrent
50090-1856-150090185601180 TABLET, FILM COATED in 1 BOTTLE (50090-1856-1) 2015-06-020000-00-00NoNoCurrent
50090-1856-25009018560230 TABLET, FILM COATED in 1 BOTTLE (50090-1856-2) 2015-06-020000-00-00NoNoCurrent
50090-1856-35009018560390 TABLET, FILM COATED in 1 BOTTLE (50090-1856-3) 2019-06-110000-00-00NoNoCurrent