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
- 27241-256_d0fe5d1b-fb0c-4c7b-af8b-cda49f2c8f7e
- Product NDC
- 27241-256
- Form
- FOR SUSPENSION
- Composition / generic term
- Pantoprazole sodium
- Labeler
- Ajanta Pharma USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230209
- Source listing expiry
- 20271231
Source-listed ingredients
- PANTOPRAZOLE SODIUM — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 FOR SUSPENSION in 1 PACKET (27241-256-11) · 27241-256-11
- 30 FOR SUSPENSION in 1 CARTON (27241-256-38) · 27241-256-38
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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