United States · FDA National Drug Code directory
Pantoprazole Sodium
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
- 0615-7629_344482ad-3ddc-4be8-9fb7-a93c355a1778
- Product NDC
- 0615-7629
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- pantoprazole sodium
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110119
- Source listing expiry
- 20261231
Source-listed ingredients
- PANTOPRAZOLE SODIUM — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-05) · 0615-7629-05
- 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-07) · 0615-7629-07
- 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-14) · 0615-7629-14
- 28 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-28) · 0615-7629-28
- 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7629-30) / 5 TABLET, DELAYED RELEASE in 1 BLISTER PACK · 0615-7629-30
- 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-39) · 0615-7629-39
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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