Deferiprone 1000 mg / 1 Tablet 150 Tablet, Coated

Reference details for licensed healthcare facility review and verification.

NDC 1100054-0711-23
Product NDC00054-0711
Generic Drug NameDeferiprone
Brand NameDeferiprone
ManufacturerHikma Pharmaceuticals USA Inc.
Strength1000 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity150 Tablet, Coated
Package Description150 TABLET, COATED in 1 BOTTLE (0054-0711-23)
Active IngredientsDeferiprone
Marketing CategoryANDA

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NDC snapshot

Deferiprone 1000 mg / 1 Tablet is tracked under NDC 00054-0711-23 and rolls up into product family 00054-0711. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 150 Tablet, Coated.
  • Manufacturer: Hikma Pharmaceuticals USA Inc..
  • Dosage form: Tablet.
  • Family size: 3 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.

Deferiprone 1000 mg / 1 Tablet 150 Tablet, Coated, NDC 00054-0711-23, is a Hikma Pharmaceuticals USA Inc. 1000 mg / 1 tablet presentation packaged as 150 Tablet, Coated.

NDC search formats

  • Canonical NDC 11: 00054-0711-23
  • Digits-only NDC 11: 00054071123
  • Possible 10-digit display formats: 0054-0711-23 (0054071123), 00054-711-23 (0005471123)

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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