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
- 85534-0061_5522a929-a1b7-d0e4-e063-6394a90ae106
- Product NDC
- 85534-0061
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Pantoprazole Sodium
- Labeler
- HAWAII REPACK, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120928
- Source listing expiry
- 20271231
Source-listed ingredients
- PANTOPRAZOLE SODIUM — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, DELAYED RELEASE in 1 BOTTLE (85534-0061-0) · 85534-0061-0
- 20 TABLET, DELAYED RELEASE in 1 BOTTLE (85534-0061-1) · 85534-0061-1
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (85534-0061-2) · 85534-0061-2
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (85534-0061-3) · 85534-0061-3
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (85534-0061-4) · 85534-0061-4
- 120 TABLET, DELAYED RELEASE in 1 BOTTLE (85534-0061-5) · 85534-0061-5
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →