NDC 0054-0142 – Acarbose

Acarbose 100 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC0054-0142

Product details

Brand name
Acarbose
Generic name
Acarbose
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078470
Marketed since
May 7, 2008
Listing expires
December 31, 2026
Pharmacologic class
alpha-Glucosidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Acarbose →

Package NDC codes (1)

Package NDCDescriptionSince
0054-0142-25100 TABLET in 1 BOTTLE (0054-0142-25)May 7, 2008

Recalls mentioning this NDC

Other Acarbose products