NDC 71335-1813 – Carvedilol

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

Human Prescription Drug

Product NDC71335-1813

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 (7)

Package NDCDescriptionSince
71335-1813-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1813-1)Jul 17, 2024
71335-1813-260 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1813-2)Jun 11, 2021
71335-1813-3100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1813-3)Sep 6, 2023
71335-1813-490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1813-4)Aug 10, 2021
71335-1813-5120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1813-5)Jul 17, 2024
71335-1813-6180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1813-6)Oct 27, 2021
71335-1813-710 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1813-7)Jul 17, 2024

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