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Methotrexate Sodium - 66758-040-02 - (Methotrexate Sodium)

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Drug Information of Methotrexate Sodium

Product NDC: 66758-040
Proprietary Name: Methotrexate Sodium
Non Proprietary Name: Methotrexate Sodium
Active Ingredient(s): 25    mg/mL & nbsp;   Methotrexate Sodium
Administration Route(s): INTRA-ARTERIAL; INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Methotrexate Sodium

Product NDC: 66758-040
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090039
Marketing Category: ANDA
Start Marketing Date: 20090601

Package Information of Methotrexate Sodium

Package NDC: 66758-040-02
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (66758-040-02) > 2 mL in 1 VIAL, SINGLE-DOSE (66758-040-01)

NDC Information of Methotrexate Sodium

NDC Code 66758-040-02
Proprietary Name Methotrexate Sodium
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (66758-040-02) > 2 mL in 1 VIAL, SINGLE-DOSE (66758-040-01)
Product NDC 66758-040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methotrexate Sodium
Dosage Form Name INJECTION, SOLUTION
Route Name INTRA-ARTERIAL; INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS
Start Marketing Date 20090601
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name METHOTREXATE SODIUM
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

Complete Information of Methotrexate Sodium


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