Eltrombopag - Olamine 50 mg / 1 Tablet 19 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

NDC 1172205-0158-19
Product NDC72205-0158
Generic Drug Nameeltrombopag olamine
Brand Nameeltrombopag
ManufacturerNovadoz Pharmaceuticals LLC
Strength50 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity19 Tablet, Film Coated
Package Description19 TABLET, FILM COATED in 1 BOTTLE (72205-158-19)
Active IngredientsEltrombopag Olamine
Marketing CategoryANDA

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NDC snapshot

eltrombopag olamine 50 mg / 1 Tablet is tracked under NDC 72205-0158-19 and rolls up into product family 72205-0158. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 19 Tablet, Film Coated.
  • Manufacturer: Novadoz Pharmaceuticals 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.

Eltrombopag - Olamine 50 mg / 1 Tablet 19 Tablet, Film Coated, NDC 72205-0158-19, is a Novadoz Pharmaceuticals LLC 50 mg / 1 tablet presentation packaged as 19 Tablet, Film Coated.

NDC search formats

  • Canonical NDC 11: 72205-0158-19
  • Digits-only NDC 11: 72205015819
  • Possible 10-digit display format: 72205-158-19 (7220515819)

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