"69339-184-03" National Drug Code (NDC)

NDC Code	69339-184-03
Package Description	30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (69339-184-03)
Product NDC	69339-184
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	2
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]