Methotrexate Sodium

Product NDC

66758-041

11-digit product format

667580041

Labeler code

66758

Product ID

66758-041_b4c82062-08eb-482e-ba9d-6423ad032a98

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methotrexate Sodium

Dosage form

INJECTION, SOLUTION

Route

INTRA-ARTERIAL; INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS

Labeler

Sandoz Inc

Application

ANDA090029

Marketing category

ANDA

Marketing start

2009-06-01

Marketing end

0000-00-00

Substance

METHOTREXATE SODIUM

Active strength

25 mg/mL

Pharmacologic classes

Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record