NDC 71335-1407 – Carvedilol

Carvedilol 3.125 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1407

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 (6)

Package NDCDescriptionSince
71335-1407-130 TABLET, FILM COATED in 1 BOTTLE (71335-1407-1)Dec 8, 2020
71335-1407-2100 TABLET, FILM COATED in 1 BOTTLE (71335-1407-2)Aug 19, 2021
71335-1407-3180 TABLET, FILM COATED in 1 BOTTLE (71335-1407-3)Sep 11, 2020
71335-1407-460 TABLET, FILM COATED in 1 BOTTLE (71335-1407-4)Nov 22, 2019
71335-1407-590 TABLET, FILM COATED in 1 BOTTLE (71335-1407-5)Nov 27, 2019
71335-1407-6120 TABLET, FILM COATED in 1 BOTTLE (71335-1407-6)Jul 9, 2024

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