NDC 50090-7890 – Carvedilol

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

Human Prescription Drug

Product NDC50090-7890

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076373
Marketed since
September 6, 2007
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
50090-7890-090 TABLET, FILM COATED in 1 BOTTLE (50090-7890-0)Feb 9, 2026

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