63629-1472 Methotrexate Sodium

Product NDC:

63629-1472

Brand Name:

Methotrexate Sodium

Generic Name:

Methotrexate sodium

Dosage Form Name:

Tablet

Administration Route:

Oral

Substances:

Name: METHOTREXATE SODIUM

Strength: 2.5

Unit: mg/1

Packages:

Code: 63629-1472-01

Description: 30 TABLET in 1 BOTTLE, PLASTIC (63629-1472-1)

Effective Date: June 4, 2014

Discontinued:

Code: 63629-1472-02

Description: 12 TABLET in 1 BOTTLE, PLASTIC (63629-1472-2)

Effective Date: Jan. 16, 2008

Discontinued:

Code: 63629-1472-03

Description: 20 TABLET in 1 BOTTLE, PLASTIC (63629-1472-3)

Effective Date: April 19, 2010

Discontinued:

Code: 63629-1472-04

Description: 100 TABLET in 1 BOTTLE, PLASTIC (63629-1472-4)

Effective Date: July 19, 2010

Discontinued:

Code: 63629-1472-05

Description: 36 TABLET in 1 BOTTLE (63629-1472-5)

Effective Date: Dec. 11, 2012

Discontinued:

Code: 63629-1472-06

Description: 24 TABLET in 1 BOTTLE (63629-1472-6)

Effective Date: Aug. 26, 2019

Discontinued:

Code: 63629-1472-07

Description: 90 TABLET in 1 BOTTLE, PLASTIC (63629-1472-7)

Effective Date: Sept. 20, 2021

Discontinued:

Code: 63629-1472-08

Description: 4 TABLET in 1 BOTTLE, PLASTIC (63629-1472-8)

Effective Date: Sept. 20, 2021

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