NDC 71335-0273 – Carvedilol

Carvedilol 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0273

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078332
Marketed since
September 5, 2007
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker; beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Carvedilol →

Package NDC codes (7)

Package NDCDescriptionSince
71335-0273-1100 TABLET, FILM COATED in 1 BOTTLE (71335-0273-1)Sep 6, 2023
71335-0273-230 TABLET, FILM COATED in 1 BOTTLE (71335-0273-2)Mar 30, 2018
71335-0273-390 TABLET, FILM COATED in 1 BOTTLE (71335-0273-3)Jul 2, 2018
71335-0273-460 TABLET, FILM COATED in 1 BOTTLE (71335-0273-4)May 7, 2018
71335-0273-5120 TABLET, FILM COATED in 1 BOTTLE (71335-0273-5)Jul 9, 2024
71335-0273-6180 TABLET, FILM COATED in 1 BOTTLE (71335-0273-6)Feb 13, 2018
71335-0273-710 TABLET, FILM COATED in 1 BOTTLE (71335-0273-7)Jul 9, 2024

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