42292-0051 Erlotinib Hydrochloride

Product NDC:

42292-0051

Brand Name:

Erlotinib Hydrochloride

Generic Name:

Erlotinib hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ERLOTINIB

Strength: 25.0

Unit: mg/1

Packages:

Code: 42292-0051-05

Description: 20 BLISTER PACK in 1 CARTON (42292-051-05) > 1 TABLET, FILM COATED in 1 BLISTER PACK (42292-051-01)

Effective Date: May 28, 2019

Discontinued: Jan. 31, 2021

SEER*Rx Category:

Chemotherapy

Major Class:

Tyrosine Kinase Inhibitor

Minor Class:

EGFR

Orphan Drug Designation:

Status:

No Longer Used

CanMED and the Oncology Toolbox