NDC 68462-164 – Carvedilol

Carvedilol 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 10 recalls

Product NDC68462-164

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078251
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 (5)

Package NDCDescriptionSince
68462-164-01100 TABLET, FILM COATED in 1 BOTTLE (68462-164-01)Sep 5, 2007
68462-164-05500 TABLET, FILM COATED in 1 BOTTLE (68462-164-05)Sep 5, 2007
68462-164-101000 TABLET, FILM COATED in 1 BOTTLE (68462-164-10)Sep 5, 2007
68462-164-18180 TABLET, FILM COATED in 1 BOTTLE (68462-164-18)Dec 10, 2014
68462-164-6060 TABLET, FILM COATED in 1 BOTTLE (68462-164-60)Sep 5, 2007

Recalls mentioning this NDC

Other Carvedilol products