70771-1522 Erlotinib - CanMED: NDC

Product NDC:

70771-1522

Brand Name:

Erlotinib

Generic Name:

Erlotinib

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ERLOTINIB HYDROCHLORIDE

Strength: 100.0

Unit: mg/1

Packages:

Code: 70771-1522-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (70771-1522-3)

Effective Date: April 30, 2020

Discontinued:

Code: 70771-1522-07

Description: 3 BLISTER PACK in 1 CARTON (70771-1522-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1522-2)

Effective Date: April 30, 2020

Discontinued:

Code: 70771-1522-09

Description: 90 TABLET, FILM COATED in 1 BOTTLE (70771-1522-9)

Effective Date: April 30, 2020

Discontinued:

SEER*Rx Category:

Chemotherapy

Major Class:

Tyrosine Kinase Inhibitor

Minor Class:

EGFR

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox