"16571-884-10" National Drug Code (NDC)

Allopurinol 1000 TABLET in 1 BOTTLE (16571-884-10)
(Rising Pharma Holdings, Inc.)

NDC Code16571-884-10
Package Description1000 TABLET in 1 BOTTLE (16571-884-10)
Product NDC16571-884
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAllopurinol
Non-Proprietary NameAllopurinol
Dosage FormTABLET
UsageORAL
Start Marketing Date20230921
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA016084
ManufacturerRising Pharma Holdings, Inc.
Substance NameALLOPURINOL
Strength200
Strength Unitmg/1
Pharmacy ClassesXanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]

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