Methotrexate

Product NDC

70518-1251

11-digit product format

705181251

Labeler code

70518

Product ID

70518-1251_9102a342-77b1-9abd-e053-2995a90ae764

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methotrexate Sodium

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA201749

Marketing category

ANDA

Marketing start

2018-06-11

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

2020-12-31

Current FDA listing

Historical FDA.report record