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"70771-1058-7" National Drug Code (NDC)
Methotrexate 100 BLISTER PACK in 1 CARTON (70771-1058-7) / 1 TABLET in 1 BLISTER PACK (70771-1058-2)
(Zydus Lifesciences Limited)
NDC Code
70771-1058-7
Package Description
100 BLISTER PACK in 1 CARTON (70771-1058-7) / 1 TABLET in 1 BLISTER PACK (70771-1058-2)
Product NDC
70771-1058
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Methotrexate
Non-Proprietary Name
Methotrexate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20170209
Marketing Category Name
ANDA
Application Number
ANDA207812
Manufacturer
Zydus Lifesciences Limited
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/70771-1058-7