NDC 65862-145 – Carvedilol

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

Human Prescription Drug 1 recall

Product NDC65862-145

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078332
Marketed since
September 5, 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 (3)

Package NDCDescriptionSince
65862-145-01100 TABLET, FILM COATED in 1 BOTTLE (65862-145-01)Sep 5, 2007
65862-145-05500 TABLET, FILM COATED in 1 BOTTLE (65862-145-05)Sep 5, 2007
65862-145-991000 TABLET, FILM COATED in 1 BOTTLE (65862-145-99)Sep 5, 2007

Recalls mentioning this NDC

Other Carvedilol products