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"70710-2009-0" National Drug Code (NDC)

Allopurinol 1000 TABLET in 1 BOTTLE (70710-2009-0)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code70710-2009-0
Package Description1000 TABLET in 1 BOTTLE (70710-2009-0)
Product NDC70710-2009
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAllopurinol
Non-Proprietary NameAllopurinol
Dosage FormTABLET
UsageORAL
Start Marketing Date20250617
Marketing Category NameANDA
Application NumberANDA210117
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameALLOPURINOL
Strength200
Strength Unitmg/1
Pharmacy ClassesXanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70710-2009-0





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