59676-578 : Prezcobix Oral Tablet, Film Coated


NDC: 59676-578
Labeler: Janssen Products Lp
Product Type: Human Prescription Drug
Drug Name:  Prezcobix
Dosage Form: Oral Tablet, Film Coated
Application #: NDA205395
Rev. Date: 


NDC Package Codes:

  • 59676-578-30: 30 TABLET, FILM COATED IN 1 BOTTLE (59676‑578‑30)

Active Ingredients:

  • Cobicistat
  • Darunavir Ethanolate

Dosage Strength:

  • 150 mg
  • 675 mg

Pharmaceutical Classes:

  • Breast Cancer Resistance Protein Inhibitors [MoA]
  • Cytochrome P450 2D6 Inhibitors [MoA]
  • Cytochrome P450 3A Inhibitor [EPC]
  • Cytochrome P450 3A Inhibitors [MoA]
  • HIV Protease Inhibitors [MoA]
  • Multidrug and Toxin Extrusion Transporter 1 Inhibitors [MoA]
  • Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA]
  • Organic Anion Transporting Polypeptide 1B3 Inhibitors [MoA]
  • P-Glycoprotein Inhibitors [MoA]
  • Protease Inhibitor [EPC]

Related Products:

Based on records with the same trade name.
  • 59676-575 Prezcobix Oral Tablet, Film Coated by Janssen Products Lp
  • 50090-1723 Prezcobix Oral Tablet, Film Coated by A-s Medication Solutions
  • 54569-6594 Prezcobix Oral Tablet, Film Coated by A-s Medication Solutions
  • 70518-0714 Prezcobix Oral Tablet, Film Coated by Remedyrepack Inc.

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.