NDC 55111-333 – Pantoprazole

Pantoprazole Sodium 40 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC55111-333

Product details

Brand name
Pantoprazole
Generic name
Pantoprazole
Labeler
Dr.Reddy's Laboratories Limited
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA077619
Marketed since
January 19, 2011
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pantoprazole →

Package NDC codes (7)

Package NDCDescriptionSince
55111-333-01100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-01)Jan 19, 2011
55111-333-05500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-05)Jan 19, 2011
55111-333-101000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-10)May 1, 2026
55111-333-3030 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-30)Jan 19, 2011
55111-333-7810 BLISTER PACK in 1 CARTON (55111-333-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)Jan 19, 2011
55111-333-813 BLISTER PACK in 1 CARTON (55111-333-81) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)Jan 19, 2011
55111-333-9090 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-90)Jan 19, 2011

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