NDC 42708-072 – Carvedilol

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

Human Prescription Drug

Product NDC42708-072

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
QPharma, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076373
Marketed since
September 6, 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 (1)

Package NDCDescriptionSince
42708-072-60 sample60 TABLET, FILM COATED in 1 BOTTLE (42708-072-60)Apr 18, 2018

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