"70710-2009-9" National Drug Code (NDC)

Allopurinol 90 TABLET in 1 BOTTLE (70710-2009-9)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code70710-2009-9
Package Description90 TABLET in 1 BOTTLE (70710-2009-9)
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]

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