Rabeprazole Sodium - Rabeprazole 20 mg / 1 Tablet 30 Tablet, Delayed Release

Reference details for licensed healthcare facility review and verification.

NDC 1165162-0724-03
Product NDC65162-0724
Generic Drug NameRabeprazole
Brand NameRabeprazole Sodium
ManufacturerAmneal Pharmaceuticals LLC
Strength20 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Delayed Release
Package Description30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-03)
Active IngredientsRabeprazole Sodium
Marketing CategoryANDA

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NDC snapshot

Rabeprazole 20 mg / 1 Tablet is tracked under NDC 65162-0724-03 and rolls up into product family 65162-0724. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Tablet, Delayed Release.
  • Manufacturer: Amneal Pharmaceuticals LLC.
  • Dosage form: Tablet.
  • Family size: 4 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.

Rabeprazole Sodium - Rabeprazole 20 mg / 1 Tablet 30 Tablet, Delayed Release, NDC 65162-0724-03, is a Amneal Pharmaceuticals LLC 20 mg / 1 tablet presentation packaged as 30 Tablet, Delayed Release.

NDC search formats

  • Canonical NDC 11: 65162-0724-03
  • Digits-only NDC 11: 65162072403
  • Possible 10-digit display formats: 65162-724-03 (6516272403), 65162-0724-3 (6516207243)

Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.

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