NDC 68001-153 – Carvedilol

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

Human Prescription Drug

Product NDC68001-153

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
BluePoint Laboratories
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
April 22, 2014
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 (2)

Package NDCDescriptionSince
68001-153-00100 TABLET, FILM COATED in 1 BOTTLE (68001-153-00)Apr 22, 2014
68001-153-03500 TABLET, FILM COATED in 1 BOTTLE (68001-153-03)Apr 22, 2014

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