NDC 51655-029 – Carvedilol

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

Human Prescription Drug

Product NDC51655-029

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
February 9, 2015
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 (3)

Package NDCDescriptionSince
51655-029-2560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-029-25)Sep 9, 2022
51655-029-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-029-26)Nov 22, 2022
51655-029-5230 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-029-52)Feb 9, 2015

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