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"70518-1398-1" National Drug Code (NDC)
Methotrexate 20 TABLET in 1 BOTTLE, PLASTIC (70518-1398-1)
(REMEDYREPACK INC.)
NDC Code
70518-1398-1
Package Description
20 TABLET in 1 BOTTLE, PLASTIC (70518-1398-1)
Product NDC
70518-1398
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Methotrexate
Non-Proprietary Name
Methotrexate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180904
Marketing Category Name
ANDA
Application Number
ANDA207812
Manufacturer
REMEDYREPACK INC.
Substance Name
METHOTREXATE
Strength
2.5
Strength Unit
mg/1
Pharmacy Classes
Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1398-1