NDC 68462-496 – deferasirox

Deferasirox 500 mg/1 · Tablet, For Suspension · Oral

Human Prescription Drug 1 recall

Product NDC68462-496

Product details

Brand name
deferasirox
Generic name
deferasirox
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Tablet, For Suspension
Route
Oral
Marketing category
ANDA · ANDA209433
Marketed since
January 6, 2020
Listing expires
December 31, 2026
Pharmacologic class
Iron Chelator

Active ingredients

Uses, dosage, side effects and warnings for Deferasirox →

Package NDC codes (1)

Package NDCDescriptionSince
68462-496-9090 TABLET, FOR SUSPENSION in 1 BOTTLE (68462-496-90)Jan 6, 2020

Recalls mentioning this NDC

Other Deferasirox products