Home > National Drug Code (NDC) > Methotrexate

Methotrexate - 55390-034-10 - (Methotrexate)

Alphabetical Index


Drug Information of Methotrexate

Product NDC: 55390-034
Proprietary Name: Methotrexate
Non Proprietary Name: Methotrexate
Active Ingredient(s): 25    mg/mL & nbsp;   Methotrexate
Administration Route(s): INTRA-ARTERIAL; INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Methotrexate

Product NDC: 55390-034
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089343
Marketing Category: ANDA
Start Marketing Date: 19960501

Package Information of Methotrexate

Package NDC: 55390-034-10
Package Description: 10 VIAL in 1 BOX, UNIT-DOSE (55390-034-10) > 10 mL in 1 VIAL

NDC Information of Methotrexate

NDC Code 55390-034-10
Proprietary Name Methotrexate
Package Description 10 VIAL in 1 BOX, UNIT-DOSE (55390-034-10) > 10 mL in 1 VIAL
Product NDC 55390-034
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methotrexate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRA-ARTERIAL; INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS
Start Marketing Date 19960501
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name METHOTREXATE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

Complete Information of Methotrexate


General Information