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: 62756-071_d19d65d9-7bab-4a6f-9a79-ed3d32bd83d9
Product NDC: 62756-071
Form: GRANULE, DELAYED RELEASE
Composition / generic term: PANTOPRAZOLE SODIUM
Labeler: Sun Pharmaceutical Industries, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20200701
Source listing expiry: 20261231

Source-listed ingredients

PANTOPRAZOLE SODIUM — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 PACKET in 1 CARTON (62756-071-64) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (62756-071-60) · 62756-071-64

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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