NDC 51655-034 – Carvedilol

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

Human Prescription Drug

Product NDC51655-034

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
August 9, 2022
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 (3)

Package NDCDescriptionSince
51655-034-2560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-25)Oct 18, 2022
51655-034-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-52)Aug 9, 2022
51655-034-83180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-83)Jan 11, 2023

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