"68382-115-05" National Drug Code (NDC)

NDC Code	68382-115-05
Package Description	500 TABLET, FILM COATED in 1 BOTTLE (68382-115-05)
Product NDC	68382-115
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Risperidone
Non-Proprietary Name	Risperidone
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20081113
Marketing Category Name	ANDA
Application Number	ANDA078040
Manufacturer	Zydus Pharmaceuticals USA Inc.
Substance Name	RISPERIDONE
Strength	2
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]