NDC 68071-2780 – Carvedilol

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

Human Prescription Drug

Product NDC68071-2780

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
September 5, 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 (3)

Package NDCDescriptionSince
68071-2780-660 TABLET, FILM COATED in 1 BOTTLE (68071-2780-6)Jun 28, 2024
68071-2780-8180 TABLET, FILM COATED in 1 BOTTLE (68071-2780-8)Jul 5, 2022
68071-2780-990 TABLET, FILM COATED in 1 BOTTLE (68071-2780-9)Jul 5, 2022

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