Pantoprazole 20 mg / 1 Tablet 1000 Tablet, Delayed Release

Reference details for licensed healthcare facility review and verification.

NDC 1155111-0332-10
Product NDC55111-0332
Generic Drug NamePantoprazole
Brand NamePantoprazole
ManufacturerDr.Reddy's Laboratories Limited
Strength20 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity1000 Tablet, Delayed Release
Package Description1000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-332-10)
Active IngredientsPantoprazole Sodium
Marketing CategoryANDA

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NDC snapshot

Pantoprazole 20 mg / 1 Tablet is tracked under NDC 55111-0332-10 and rolls up into product family 55111-0332. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 1000 Tablet, Delayed Release.
  • Manufacturer: Dr.Reddy's Laboratories Limited.
  • Dosage form: Tablet.
  • Family size: 7 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 20 mg / 1 Tablet 1000 Tablet, Delayed Release, NDC 55111-0332-10, is a Dr.Reddy's Laboratories Limited 20 mg / 1 tablet presentation packaged as 1000 Tablet, Delayed Release.

NDC search formats

  • Canonical NDC 11: 55111-0332-10
  • Digits-only NDC 11: 55111033210
  • Possible 10-digit display format: 55111-332-10 (5511133210)

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