NDC 51655-030 – Carvedilol

Carvedilol 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51655-030

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
March 23, 2022
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 (4)

Package NDCDescriptionSince
51655-030-2560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-25)Apr 13, 2022
51655-030-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-26)Jul 14, 2022
51655-030-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-52)Mar 23, 2022
51655-030-83180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-83)Apr 13, 2022

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