NDC 68071-3970 – Carvedilol

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

Human Prescription Drug

Product NDC68071-3970

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078165
Marketed since
July 29, 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 (1)

Package NDCDescriptionSince
68071-3970-660 TABLET, FILM COATED in 1 BOTTLE (68071-3970-6)Feb 26, 2026

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