Haloperidol

Product NDC
72162-1688
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Haloperidol
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA071173
Marketing category
ANDA
Substance
HALOPERIDOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-1688-1100 TABLET in 1 BOTTLE (72162-1688-1) 2024-01-11NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Haloperidol Tablets, USPBryant Ranch Prepack2024-01-11HUMAN PRESCRIPTION DRUG LABEL100