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Methotrexate - Medication Information

Product NDC Code 70771-1058
Drug Name

Methotrexate

Type Generic
Pharm Class Folate Analog Metabolic Inhibitor [EPC],
Folic Acid Metabolism Inhibitors [MoA]
Active Ingredients
Methotrexate 2.5 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 105585
Application Number ANDA207812
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1058-0 1000 tablet in 1 bottle (70771-1058-0)
70771-1058-1 100 tablet in 1 bottle (70771-1058-1)
70771-1058-3 36 tablet in 1 bottle (70771-1058-3)
70771-1058-5 500 tablet in 1 bottle (70771-1058-5)
70771-1058-7 100 blister pack in 1 carton (70771-1058-7) / 1 tablet in 1 blister pack (70771-1058-2)
70771-1058-9 90 tablet in 1 bottle (70771-1058-9)
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Spl product data elements

Usually a list of ingredients in a drug product.
Methotrexate Methotrexate METHOTREXATE METHOTREXATE ANHYDROUS LACTOSE CELLULOSE, MICROCRYSTALLINE LACTOSE MONOHYDRATE MAGNESIUM STEARATE STARCH, CORN YELLOW ROUND L2

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1058-1 Methotrexate tablets, USP 2.5 mg Rx only 36 tablets Methotrexate tablets, USP

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API