NDC 71335-1533 – Carvedilol

Carvedilol 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1533

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078251
Marketed since
September 5, 2007
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Blocker; beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Carvedilol →

Package NDC codes (7)

Package NDCDescriptionSince
71335-1533-130 TABLET, FILM COATED in 1 BOTTLE (71335-1533-1)Aug 10, 2011
71335-1533-260 TABLET, FILM COATED in 1 BOTTLE (71335-1533-2)Aug 10, 2011
71335-1533-3100 TABLET, FILM COATED in 1 BOTTLE (71335-1533-3)Aug 10, 2011
71335-1533-490 TABLET, FILM COATED in 1 BOTTLE (71335-1533-4)Aug 10, 2011
71335-1533-5120 TABLET, FILM COATED in 1 BOTTLE (71335-1533-5)Aug 10, 2011
71335-1533-6180 TABLET, FILM COATED in 1 BOTTLE (71335-1533-6)Aug 10, 2011
71335-1533-710 TABLET, FILM COATED in 1 BOTTLE (71335-1533-7)Jun 5, 2026

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