Carvedilol

Product NDC
43547-256
11-digit product format
435470256
Labeler code
43547
Product ID
43547-256_9db9f3d1-f2f8-456d-b4ff-0de943ccb448
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carvedilol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Solco Healthcare US LLC
Application
ANDA078384
Marketing category
ANDA
Marketing start
2010-06-01
Marketing end
2020-08-01
Substance
CARVEDILOL
Active strength
13 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
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e148a93c-bfff-2735-e6c0-0739297b4596Product name320180705
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
32d6365f-9f0e-0782-b719-48e651893fb7Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
200032carvedilol 12.5 MG Oral TabletPSN25566ff0-3747-4f32-8d4f-de0dfbbb55301
200032carvedilol 12.5 MG Oral TabletSCD25566ff0-3747-4f32-8d4f-de0dfbbb55301