NDC 51655-397 – Carvedilol

Carvedilol 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51655-397

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
July 8, 2020
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 (4)

Package NDCDescriptionSince
51655-397-2560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-25)Feb 9, 2022
51655-397-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-26)Jul 8, 2020
51655-397-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-52)Feb 9, 2022
51655-397-83180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-83)Mar 10, 2023

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