NDC 0615-8387 – Carvedilol

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

Human Prescription Drug

Product NDC0615-8387

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076373
Marketed since
September 6, 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 (2)

Package NDCDescriptionSince
0615-8387-0515 TABLET, FILM COATED in 1 BLISTER PACK (0615-8387-05)Aug 8, 2023
0615-8387-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8387-39)Feb 23, 2021

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