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"71921-240-33" National Drug Code (NDC)

Allopurinol 30 TABLET in 1 BOTTLE (71921-240-33)
(Florida Pharmaceutical Products, LLC)

NDC Code71921-240-33
Package Description30 TABLET in 1 BOTTLE (71921-240-33)
Product NDC71921-240
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAllopurinol
Non-Proprietary NameAllopurinol
Dosage FormTABLET
UsageORAL
Start Marketing Date20231031
Marketing Category NameANDA
Application NumberANDA204467
ManufacturerFlorida Pharmaceutical Products, LLC
Substance NameALLOPURINOL
Strength100
Strength Unitmg/1
Pharmacy ClassesXanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71921-240-33





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