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METHOTREXATE - 54868-0173-0 - (methotrexate)

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Drug Information of METHOTREXATE

Product NDC: 54868-0173
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: 54868-0173
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089343
Marketing Category: ANDA
Start Marketing Date: 20030326

Package Information of METHOTREXATE

Package NDC: 54868-0173-0
Package Description: 2 mL in 1 VIAL (54868-0173-0)

NDC Information of METHOTREXATE

NDC Code 54868-0173-0
Proprietary Name METHOTREXATE
Package Description 2 mL in 1 VIAL (54868-0173-0)
Product NDC 54868-0173
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 20030326
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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


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