NDC 71335-2101 – Carvedilol

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

Human Prescription Drug

Product NDC71335-2101

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
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 (8)

Package NDCDescriptionSince
71335-2101-130 TABLET, FILM COATED in 1 BOTTLE (71335-2101-1)Apr 3, 2024
71335-2101-260 TABLET, FILM COATED in 1 BOTTLE (71335-2101-2)Jul 14, 2022
71335-2101-3100 TABLET, FILM COATED in 1 BOTTLE (71335-2101-3)Jul 21, 2022
71335-2101-4180 TABLET, FILM COATED in 1 BOTTLE (71335-2101-4)Nov 17, 2023
71335-2101-590 TABLET, FILM COATED in 1 BOTTLE (71335-2101-5)Feb 12, 2024
71335-2101-6120 TABLET, FILM COATED in 1 BOTTLE (71335-2101-6)Jul 8, 2022
71335-2101-725 TABLET, FILM COATED in 1 BOTTLE (71335-2101-7)Apr 3, 2024
71335-2101-810 TABLET, FILM COATED in 1 BOTTLE (71335-2101-8)Apr 3, 2024

Other Carvedilol products