NDC 0093-7296 – Carvedilol

Carvedilol 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0093-7296

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Teva Pharmaceuticals USA, Inc.
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
0093-7296-01100 TABLET, FILM COATED in 1 BOTTLE (0093-7296-01)Sep 6, 2007
0093-7296-05500 TABLET, FILM COATED in 1 BOTTLE (0093-7296-05)Dec 2, 2008

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