NDC 68071-4600 – Carvedilol

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

Human Prescription Drug

Product NDC68071-4600

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078332
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 (4)

Package NDCDescriptionSince
68071-4600-330 TABLET, FILM COATED in 1 BOTTLE (68071-4600-3)Oct 17, 2018
68071-4600-660 TABLET, FILM COATED in 1 BOTTLE (68071-4600-6)Oct 17, 2018
68071-4600-8180 TABLET, FILM COATED in 1 BOTTLE (68071-4600-8)Oct 17, 2018
68071-4600-990 TABLET, FILM COATED in 1 BOTTLE (68071-4600-9)Oct 17, 2018

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