"68788-2115-3" National Drug Code (NDC)

Allopurinol 30 TABLET in 1 BOTTLE (68788-2115-3)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-2115-3
Package Description30 TABLET in 1 BOTTLE (68788-2115-3)
Product NDC68788-2115
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAllopurinol
Non-Proprietary NameAllopurinol
Dosage FormTABLET
UsageORAL
Start Marketing Date20091001
Marketing Category NameANDA
Application NumberANDA071586
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameALLOPURINOL
Strength100
Strength Unitmg/1
Pharmacy ClassesXanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]

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