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"71335-2221-5" National Drug Code (NDC)
Methotrexate 36 TABLET in 1 BOTTLE (71335-2221-5)
(Bryant Ranch Prepack)
NDC Code
71335-2221-5
Package Description
36 TABLET in 1 BOTTLE (71335-2221-5)
Product NDC
71335-2221
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Methotrexate
Non-Proprietary Name
Methotrexate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200130
Marketing Category Name
ANDA
Application Number
ANDA210454
Manufacturer
Bryant Ranch Prepack
Substance Name
METHOTREXATE SODIUM
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/71335-2221-5