Citalopram Hydrobromide

Product NDC
50090-6947
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Citalopram Hydrobromide
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078216
Marketing category
ANDA
Substance
CITALOPRAM HYDROBROMIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6947-090 TABLET in 1 BOTTLE (50090-6947-0) 2023-12-18NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Citalopram HydrobromideA-S Medication Solutions2023-12-26HUMAN PRESCRIPTION DRUG LABEL1