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"16571-885-01" National Drug Code (NDC)

Allopurinol 100 TABLET in 1 BOTTLE (16571-885-01)
(Rising Pharma Holdings, Inc.)

NDC Code16571-885-01
Package Description100 TABLET in 1 BOTTLE (16571-885-01)
Product NDC16571-885
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
Strength300
Strength Unitmg/1
Pharmacy ClassesXanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16571-885-01





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