70771-1058 Methotrexate

Product NDC:

70771-1058

Brand Name:

Methotrexate

Generic Name:

Methotrexate

Dosage Form Name:

Tablet

Administration Route:

Oral

Substances:

Name: METHOTREXATE

Strength: 2.5

Unit: mg/1

Packages:

Code: 70771-1058-00

Description: 1000 TABLET in 1 BOTTLE (70771-1058-0)

Effective Date: Feb. 9, 2017

Discontinued:

Code: 70771-1058-01

Description: 100 TABLET in 1 BOTTLE (70771-1058-1)

Effective Date: Feb. 9, 2017

Discontinued:

Code: 70771-1058-02

Description:

Effective Date: Feb. 9, 2017

Discontinued:

Code: 70771-1058-03

Description: 36 TABLET in 1 BOTTLE (70771-1058-3)

Effective Date: Feb. 9, 2017

Discontinued:

Code: 70771-1058-05

Description: 500 TABLET in 1 BOTTLE (70771-1058-5)

Effective Date: Feb. 9, 2017

Discontinued:

Code: 70771-1058-07

Description: 100 BLISTER PACK in 1 CARTON (70771-1058-7) / 1 TABLET in 1 BLISTER PACK (70771-1058-2)

Effective Date: Feb. 9, 2017

Discontinued:

Code: 70771-1058-09

Description: 90 TABLET in 1 BOTTLE (70771-1058-9)

Effective Date: Feb. 9, 2017

Discontinued:

SEER*Rx Category:

Chemotherapy

Major Class:

Antimetabolite

Minor Class:

Folic Acid Analog

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox

CanMED: NDC