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: 31722-712_48f42a12-2eac-e5dd-e063-6294a90aa92d
Product NDC: 31722-712
Form: TABLET, DELAYED RELEASE
Composition / generic term: PANTOPRAZOLE
Labeler: Camber Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20140910
Source listing expiry: 20271231

Source-listed ingredients

PANTOPRAZOLE SODIUM — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (31722-712-31) · 31722-712-31
10 TABLET, DELAYED RELEASE in 1 CARTON (31722-712-32) · 31722-712-32
90 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-712-90) · 31722-712-90

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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