"69339-182-03" National Drug Code (NDC)

NDC Code	69339-182-03
Package Description	30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (69339-182-03)
Product NDC	69339-182
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Risperidone
Non-Proprietary Name	Risperidone
Dosage Form	TABLET, ORALLY DISINTEGRATING
Usage	ORAL
Start Marketing Date	20231014
Marketing Category Name	ANDA
Application Number	ANDA091537
Manufacturer	Natco Pharma USA LLC
Substance Name	RISPERIDONE
Strength	.5
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]