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"0703-3673-01" National Drug Code (NDC)
Methotrexate 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3673-01) > 4 mL in 1 VIAL, SINGLE-DOSE
(Teva Parenteral Medicines, Inc.)
NDC Code
0703-3673-01
Package Description
1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3673-01) > 4 mL in 1 VIAL, SINGLE-DOSE
Product NDC
0703-3673
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Methotrexate
Non-Proprietary Name
Methotrexate Sodium
Dosage Form
INJECTION, SOLUTION
Usage
INTRA-ARTERIAL; INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS
Start Marketing Date
20120801
Marketing Category Name
ANDA
Application Number
ANDA200171
Manufacturer
Teva Parenteral Medicines, Inc.
Substance Name
METHOTREXATE SODIUM
Strength
25
Strength Unit
mg/mL
Pharmacy Classes
Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0703-3673-01