NDC 63304-967

Pantoprazole Sodium 20 mg tablet, delayed release

On the label: Ranbaxy Laboratories Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ohm Laboratories Inc.New Brunswick, NJ, United StatesMakes it No problems foundOct 31, 2024 · 22 inspections
Ranbaxy laboratories Limited ToansaLocation not on fileMakes the active ingredient Not inspected on record

Product details

Generic drug
Pantoprazole: every company that makes it
Form
tablet, delayed release
Strength
20 mg
Approval
ANDA ANDA200794
On the market since
May 2, 2012
Package NDCs
63304-967-10 63304-967-77 63304-967-90
Official label
DailyMed (National Library of Medicine), updated Apr 20, 2015

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