00378-7132 Erlotinib Hydrochloride

Product NDC:

00378-7132

Brand Name:

Erlotinib Hydrochloride

Generic Name:

erlotinib hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ERLOTINIB

Strength: 100.0

Unit: mg/1

Packages:

Code: 00378-7132-93

Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7132-93)

Effective Date: May 9, 2019

Discontinued: Nov. 30, 2022

SEER*Rx Category:

Chemotherapy

Major Class:

Tyrosine Kinase Inhibitor

Minor Class:

EGFR

Orphan Drug Designation:

Status:

No Longer Used

CanMED and the Oncology Toolbox