Methotrexate

Product NDC

21695-111

11-digit product format

216950111

Labeler code

21695

Product ID

21695-111_fce17e4f-926c-4b50-8fd6-f415d1a13570

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methotrexate sodium

Dosage form

TABLET

Route

ORAL

Labeler

Rebel Distributors Corp

Application

ANDA081099

Marketing category

ANDA

Marketing start

1990-10-15

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record