NDC 71335-1457 – Carvedilol

Carvedilol 6.25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1457

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078384
Marketed since
October 1, 2016
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 (8)

Package NDCDescriptionSince
71335-1457-130 TABLET, FILM COATED in 1 BOTTLE (71335-1457-1)Feb 3, 2020
71335-1457-260 TABLET, FILM COATED in 1 BOTTLE (71335-1457-2)Jan 31, 2020
71335-1457-3100 TABLET, FILM COATED in 1 BOTTLE (71335-1457-3)Nov 15, 2021
71335-1457-4180 TABLET, FILM COATED in 1 BOTTLE (71335-1457-4)Jan 2, 2020
71335-1457-590 TABLET, FILM COATED in 1 BOTTLE (71335-1457-5)Feb 6, 2020
71335-1457-6120 TABLET, FILM COATED in 1 BOTTLE (71335-1457-6)Jul 15, 2024
71335-1457-725 TABLET, FILM COATED in 1 BOTTLE (71335-1457-7)Jul 15, 2024
71335-1457-810 TABLET, FILM COATED in 1 BOTTLE (71335-1457-8)Jul 15, 2024

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