NDC 68382-092 – Carvedilol

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

Human Prescription Drug 3 recalls

Product NDC68382-092

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Zydus Pharmaceuticals USA Inc.
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 (3)

Package NDCDescriptionSince
68382-092-01100 TABLET, FILM COATED in 1 BOTTLE (68382-092-01)Sep 5, 2007
68382-092-05500 TABLET, FILM COATED in 1 BOTTLE (68382-092-05)Sep 5, 2007
68382-092-1728 TABLET, FILM COATED in 1 BOTTLE (68382-092-17)Sep 5, 2007

Recalls mentioning this NDC

Other Carvedilol products