METHOTREXATE

Product NDC

66336-338

11-digit product format

663360338

Labeler code

66336

Product ID

66336-338_1239c290-23b1-4b83-97b9-d9e5e45fa30b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

METHOTREXATE

Dosage form

TABLET

Route

ORAL

Labeler

Dispensing Solutions, Inc.

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