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"70710-2009-9" National Drug Code (NDC)
Allopurinol 90 TABLET in 1 BOTTLE (70710-2009-9)
(Zydus Pharmaceuticals (USA) Inc.)
NDC Code
70710-2009-9
Package Description
90 TABLET in 1 BOTTLE (70710-2009-9)
Product NDC
70710-2009
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Allopurinol
Non-Proprietary Name
Allopurinol
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20250617
Marketing Category Name
ANDA
Application Number
ANDA210117
Manufacturer
Zydus Pharmaceuticals (USA) Inc.
Substance Name
ALLOPURINOL
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70710-2009-9