NDC 50742-366 – Gefitinib

Gefitinib 250 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC50742-366

Product details

Brand name
Gefitinib
Generic name
Gefitinib
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA211591
Marketed since
April 27, 2023
Listing expires
December 31, 2026
Pharmacologic class
Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Gefitinib →

Package NDC codes (1)

Package NDCDescriptionSince
50742-366-3030 TABLET, COATED in 1 BOTTLE (50742-366-30)Apr 27, 2023

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