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Methotrexate - 0069-0148-01 - (Methotrexate)

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Drug Information of Methotrexate

Product NDC: 0069-0148
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
Coding System: National Drug Codes(NDC)

Labeler Information of Methotrexate

Product NDC: 0069-0148
Labeler Name: Pfizer Laboratories Div Pfizer Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201529
Marketing Category: ANDA
Start Marketing Date: 20120330

Package Information of Methotrexate

Package NDC: 0069-0148-01
Package Description: 10 mL in 1 VIAL (0069-0148-01)

NDC Information of Methotrexate

NDC Code 0069-0148-01
Proprietary Name Methotrexate
Package Description 10 mL in 1 VIAL (0069-0148-01)
Product NDC 0069-0148
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methotrexate
Dosage Form Name INJECTION
Route Name INTRA-ARTERIAL; INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS
Start Marketing Date 20120330
Marketing Category Name ANDA
Labeler Name Pfizer Laboratories Div Pfizer 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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