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FDA Drug information

Methotrexate

Read time: 1 mins
Marketing start date: 14 Jul 2024

Summary of product characteristics


Effective Time

20221031

Version

5

Spl Product Data Elements

Methotrexate Methotrexate METHOTREXATE METHOTREXATE ANHYDROUS LACTOSE CELLULOSE, MICROCRYSTALLINE LACTOSE MONOHYDRATE MAGNESIUM STEARATE STARCH, CORN YELLOW ROUND L2

Application Number

ANDA207812

Brand Name

Methotrexate

Generic Name

Methotrexate

Product Ndc

70771-1058

Product Type

HUMAN PRESCRIPTION DRUG

Route

ORAL

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1058-1 Methotrexate tablets, USP 2.5 mg Rx only 36 tablets Methotrexate tablets, USP

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