RISPERIDONE

Product NDC
50090-3341
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
RISPERIDONE
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA201003
Marketing category
ANDA
Substance
RISPERIDONE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-3341-030 TABLET in 1 BOTTLE (50090-3341-0) 2018-01-22NoHistorical
50090-3341-160 TABLET in 1 BOTTLE (50090-3341-1) 2023-11-06NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
RISPERIDONEA-S Medication Solutions2024-01-04Human Prescription Drug Label21