70069-848 : Rilpivirine 25 mg Oral Tablet, Film Coated


NDC: 70069-848
Labeler: Somerset Therapeutics, LLC
Product Type: Human Prescription Drug
Drug Name:  Rilpivirine
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA218798
Rev. Date: 


NDC Package Codes:

  • 70069-848-30: 30 TABLET, FILM COATED IN 1 BOTTLE (70069‑848‑30)

Active Ingredients:

  • Rilpivirine Hydrochloride

Dosage Strength:

  • 25 mg

Pharmaceutical Classes:

  • Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
  • Non-Nucleoside Analog [EXT]
  • Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]

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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.