METHOTREXATE

Product NDC

42254-110

11-digit product format

422540110

Labeler code

42254

Product ID

42254-110_03c66d8c-186a-4923-9a32-07ab07d472ad

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

METHOTREXATE

Dosage form

TABLET

Route

ORAL

Labeler

Rebel Distributors Corp

Application

NDA008085

Marketing category

NDA

Marketing start

1953-12-07

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

2017-12-31

Current FDA listing

Historical FDA.report record