NDC 60687-538 – Febuxostat

Febuxostat 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC60687-538

Product details

Brand name
Febuxostat
Generic name
Febuxostat
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205467
Marketed since
September 2, 2021
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Febuxostat →

Package NDC codes (1)

Package NDCDescriptionSince
60687-538-2130 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-538-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-538-11)Sep 2, 2021

Recalls mentioning this NDC

Other Febuxostat products