NDC 70518-1826 – Carvedilol

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

Human Prescription Drug 1 recall

Product NDC70518-1826

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
January 26, 2019
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
70518-1826-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-1826-0)Jan 26, 2019
70518-1826-1180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1826-1)Mar 13, 2019

Recalls mentioning this NDC

Other Carvedilol products