Pantoprazole Sodium - Pantoprazole 20 mg / 1 Tablet 1800 Tablet, Delayed Release

Reference details for licensed healthcare facility review and verification.

NDC 1171610-0659-42
Product NDC71610-0659
Generic Drug NamePantoprazole
Brand NamePantoprazole Sodium
ManufacturerAphena Pharma Solutions - Tennessee, LLC
Strength20 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity1800 Tablet, Delayed Release
Package Description1800 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-659-42)
Active IngredientsPantoprazole Sodium
Marketing CategoryANDA

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NDC snapshot

Pantoprazole 20 mg / 1 Tablet is tracked under NDC 71610-0659-42 and rolls up into product family 71610-0659. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 1800 Tablet, Delayed Release.
  • Manufacturer: Aphena Pharma Solutions - Tennessee, LLC.
  • Dosage form: Tablet.
  • Family size: 2 indexed presentations.

Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Alternate presentations in this family

These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.

Pantoprazole Sodium - Pantoprazole 20 mg / 1 Tablet 1800 Tablet, Delayed Release, NDC 71610-0659-42, is a Aphena Pharma Solutions - Tennessee, LLC 20 mg / 1 tablet presentation packaged as 1800 Tablet, Delayed Release.

NDC search formats

  • Canonical NDC 11: 71610-0659-42
  • Digits-only NDC 11: 71610065942
  • Possible 10-digit display format: 71610-659-42 (7161065942)

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