VARENICLINE

Product NDC
50090-6446
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
VARENICLINE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA201962
Marketing category
ANDA
Substance
VARENICLINE TARTRATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6446-056 TABLET, FILM COATED in 1 BOTTLE (50090-6446-0) 2023-04-20NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
VARENICLINEA-S Medication Solutions2023-04-25HUMAN PRESCRIPTION DRUG LABEL1