METHOTREXATE SODIUM

Product NDC

75840-111

11-digit product format

758400111

Labeler code

75840

Product ID

75840-111_72b163e6-9f58-44a0-bc51-a804036b7da1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

METHOTREXATE SODIUM

Dosage form

TABLET

Route

ORAL

Labeler

GenPak Solutions LLC

Application

NDA008085

Marketing category

NDA

Marketing start

2012-10-01

Marketing end

0000-00-00

Substance

METHOTREXATE SODIUM

Active strength

3 mg/1

Pharmacologic classes

Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record