Pantoprazole Sodium

Product NDC
60760-646
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pantoprazole Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
Application
ANDA202038
Marketing category
ANDA
Substance
PANTOPRAZOLE SODIUM
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
60760-646-3030 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-646-30) 2022-08-250000-00-00NoCurrent