61958-1901 : Genvoya Oral Tablet


NDC: 61958-1901
Labeler: Gilead Sciences, Inc.
Product Type: Human Prescription Drug
Drug Name:  Genvoya
Dosage Form: Oral Tablet
Application #: NDA207561
Rev. Date: 


Appearance:


Markings: GSI;510
Shapes:  Oval
Colors:  Green
Size (mm): 19
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 61958-1901-1: 30 TABLET IN 1 BOTTLE, PLASTIC (61958‑1901‑1)

Active Ingredients:

  • Elvitegravir
  • Cobicistat
  • Emtricitabine
  • Tenofovir Alafenamide Fumarate

Dosage Strength:

  • 150 mg
  • 150 mg
  • 200 mg
  • 10 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Cellulose, Microcrystalline
  • Hydroxypropyl Cellulose (Type H)
  • Sodium Lauryl Sulfate
  • Croscarmellose Sodium
  • Water
  • Magnesium Stearate
  • Polyvinyl Alcohol
  • Titanium Dioxide
  • Polyethylene Glycols
  • Talc
  • Indigotindisulfonate Sodium
  • Ferric Oxide Yellow

Pharmaceutical Classes:

  • HIV Integrase Inhibitors [MoA]
  • Human Immunodeficiency Virus Integrase Strand Transfer Inhibitor [EPC]
  • Cytochrome P450 2C9 Inducers [MoA]
  • Cytochrome P450 3A Inhibitors [MoA]
  • Cytochrome P450 3A Inhibitor [EPC]
  • P-Glycoprotein Inhibitors [MoA]
  • Cytochrome P450 2D6 Inhibitors [MoA]
  • Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA]
  • Organic Anion Transporting Polypeptide 1B3 Inhibitors [MoA]
  • Breast Cancer Resistance Protein Inhibitors [MoA]
  • Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
  • Nucleoside Analog [Chemical/Ingredient]
  • Nucleoside Reverse Transcriptase Inhibitors [MoA]
  • Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]

Related Products:

Based on records with the same trade name.
  • 50090-2279 Genvoya Oral Tablet by A-s Medication Solutions
  • 70518-0568 Genvoya Oral Tablet by Remedyrepack Inc.

NDC QR Code

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NDC 61958-1901 QR Code

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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.