METHOTREXATE

Product NDC

70518-0223

11-digit product format

705180223

Labeler code

70518

Product ID

70518-0223_9fdaa97f-d421-7916-e053-2a95a90a09e2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

METHOTREXATE

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA008085

Marketing category

NDA

Marketing start

2017-02-15

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

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record