NDC 71335-2033 – Carvedilol

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

Human Prescription Drug

Product NDC71335-2033

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078165
Marketed since
July 29, 2021
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
71335-2033-130 TABLET, FILM COATED in 1 BOTTLE (71335-2033-1)Feb 10, 2022
71335-2033-260 TABLET, FILM COATED in 1 BOTTLE (71335-2033-2)Feb 10, 2022
71335-2033-3100 TABLET, FILM COATED in 1 BOTTLE (71335-2033-3)Feb 10, 2022
71335-2033-4180 TABLET, FILM COATED in 1 BOTTLE (71335-2033-4)Feb 10, 2022
71335-2033-590 TABLET, FILM COATED in 1 BOTTLE (71335-2033-5)Feb 10, 2022
71335-2033-6120 TABLET, FILM COATED in 1 BOTTLE (71335-2033-6)Feb 10, 2022
71335-2033-725 TABLET, FILM COATED in 1 BOTTLE (71335-2033-7)Feb 10, 2022
71335-2033-810 TABLET, FILM COATED in 1 BOTTLE (71335-2033-8)Feb 10, 2022

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