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"0703-3675-01" National Drug Code (NDC)

Methotrexate 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3675-01) / 10 mL in 1 VIAL, SINGLE-DOSE
(Teva Parenteral Medicines, Inc.)

NDC Code0703-3675-01
Package Description1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3675-01) / 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC0703-3675
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormINJECTION, SOLUTION
UsageINTRA-ARTERIAL; INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS
Start Marketing Date20120801
Marketing Category NameANDA
Application NumberANDA040843
ManufacturerTeva Parenteral Medicines, Inc.
Substance NameMETHOTREXATE SODIUM
Strength25
Strength Unitmg/mL
Pharmacy ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]

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