NDC 51655-713 – Carvedilol

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

Human Prescription Drug

Product NDC51655-713

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078384
Marketed since
May 28, 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 (2)

Package NDCDescriptionSince
51655-713-2560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-713-25)Apr 15, 2022
51655-713-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-713-52)May 28, 2021

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