"13107-121-10" National Drug Code (NDC)

Risperidone 10 BLISTER PACK in 1 CARTON (13107-121-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Aurolife Pharma LLC)

NDC Code13107-121-10
Package Description10 BLISTER PACK in 1 CARTON (13107-121-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC13107-121
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRisperidone
Non-Proprietary NameRisperidone
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20091025
Marketing Category NameANDA
Application NumberANDA078269
ManufacturerAurolife Pharma LLC
Substance NameRISPERIDONE
Strength1
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

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