Pantoprazole Sodium

Product NDC
50090-5378
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pantoprazole Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA202038
Marketing category
ANDA
Substance
PANTOPRAZOLE SODIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-5378-030 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5378-0) 2020-11-19NoHistorical
50090-5378-190 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5378-1) 2020-11-19NoHistorical

Related DailyMed Labels