NDC 67184-0531 – Gefitinib

Gefitinib 250 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC67184-0531

Product details

Brand name
Gefitinib
Generic name
Gefitinib
Labeler
Qilu Pharmaceutical Co., Ltd.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA211591
Marketed since
February 13, 2023
Listing expires
December 31, 2026
Pharmacologic class
Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Gefitinib →

Package NDC codes (3)

Package NDCDescriptionSince
67184-0531-130 TABLET, COATED in 1 BOTTLE (67184-0531-1)Feb 13, 2023
67184-0531-2500 TABLET, COATED in 1 BOTTLE (67184-0531-2)Feb 13, 2023
67184-0531-33 BLISTER PACK in 1 CARTON (67184-0531-3) / 10 TABLET, COATED in 1 BLISTER PACKFeb 13, 2023

Other Gefitinib products