60219-1145 : Darunavir 800 mg Oral Tablet, Film Coated


NDC: 60219-1145
Labeler: Amneal Pharmaceuticals Ny LLC
Product Type: Human Prescription Drug
Drug Name:  Darunavir
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA212493
Rev. Date: 


NDC Package Codes:

  • 60219-1145-3: 1 BOTTLE, PLASTIC IN 1 CARTON (60219‑1145‑3) / 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC

Active Ingredients:

  • Darunavir

Dosage Strength:

  • 800 mg

Pharmaceutical Classes:

  • Cytochrome P450 2D6 Inhibitors [MoA]
  • Cytochrome P450 3A Inhibitors [MoA]
  • HIV Protease Inhibitors [MoA]
  • Protease Inhibitor [EPC]

Related Products:

Based on records with the same trade name.
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  • 59651-086 Darunavir 800 mg Oral Tablet, Film Coated by Aurobindo Pharma Limited
  • 68180-345 Darunavir 600 mg Oral Tablet, Film Coated by Lupin Pharmaceuticals, Inc.
  • 68180-346 Darunavir 800 mg Oral Tablet, Film Coated by Lupin Pharmaceuticals, Inc.
  • 72205-184 Darunavir 600 mg Oral Tablet, Film Coated by Novadoz Pharmaceuticals LLC
  • 72205-185 Darunavir 800 mg Oral Tablet, Film Coated by Novadoz Pharmaceuticals LLC
  • 76282-737 Darunavir 600 mg Oral Tablet by Exelan Pharmaceuticals Inc.
  • 76282-738 Darunavir 800 mg Oral Tablet by Exelan Pharmaceuticals 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.