ZOLPIDEM TARTRATE

Product NDC
60760-819
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Zolpidem Tartrate
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
Application
ANDA078970
Marketing category
ANDA
Substance
ZOLPIDEM TARTRATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
60760-819-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-819-30) 2024-08-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ZOLPIDEM TARTRATEST. MARY'S MEDICAL PARK PHARMACY2024-09-06HUMAN PRESCRIPTION DRUG LABEL1