United States · FDA National Drug Code directory
Pantoprazole
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 55111-333_c0575fc6-20c4-12a6-10b7-1af65cac1ee0
- Product NDC
- 55111-333
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Pantoprazole
- Labeler
- Dr.Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110119
- Source listing expiry
- 20271231
Source-listed ingredients
- PANTOPRAZOLE SODIUM — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-01) · 55111-333-01
- 500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-05) · 55111-333-05
- 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-10) · 55111-333-10
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-30) · 55111-333-30
- 10 BLISTER PACK in 1 CARTON (55111-333-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79) · 55111-333-78
- 3 BLISTER PACK in 1 CARTON (55111-333-81) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79) · 55111-333-81
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-90) · 55111-333-90
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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