0173-0909 : Zejula 100 mg Oral Tablet, Film Coated


NDC: 0173-0909
Labeler: Glaxosmithkline LLC
Product Type: Human Prescription Drug
Drug Name:  Zejula
Dosage Form: Oral Tablet, Film Coated
Application #: NDA214876
Rev. Date: 


NDC Package Codes:

  • 0173-0909-13: 30 TABLET, FILM COATED IN 1 BOTTLE (0173‑0909‑13)

Active Ingredients:

  • Niraparib Tosylate Monohydrate

Dosage Strength:

  • 100 mg

Pharmaceutical Classes:

  • Poly(ADP-Ribose) Polymerase Inhibitor [EPC]
  • Poly(ADP-Ribose) Polymerase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 0173-0912 Zejula 200 mg Oral Tablet, Film Coated by Glaxosmithkline LLC
  • 0173-0915 Zejula 300 mg Oral Tablet, Film Coated by Glaxosmithkline LLC
  • 69656-103 Zejula 100 mg Oral Capsule by Tesaro, Inc.

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