NDC 71335-1623 – Carvedilol

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

Human Prescription Drug

Product NDC71335-1623

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
September 5, 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 (7)

Package NDCDescriptionSince
71335-1623-1100 TABLET, FILM COATED in 1 BOTTLE (71335-1623-1)Sep 5, 2007
71335-1623-230 TABLET, FILM COATED in 1 BOTTLE (71335-1623-2)Sep 5, 2007
71335-1623-390 TABLET, FILM COATED in 1 BOTTLE (71335-1623-3)Sep 5, 2007
71335-1623-460 TABLET, FILM COATED in 1 BOTTLE (71335-1623-4)Sep 5, 2007
71335-1623-5120 TABLET, FILM COATED in 1 BOTTLE (71335-1623-5)Sep 5, 2007
71335-1623-6180 TABLET, FILM COATED in 1 BOTTLE (71335-1623-6)Sep 5, 2007
71335-1623-710 TABLET, FILM COATED in 1 BOTTLE (71335-1623-7)Sep 5, 2007

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