Rilpivirine 70069-0848

Product NDC

70069-0848

Manufacturer: Somerset Therapeutics, Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 30, 2026
Listing Expires: December 31, 2027
Application: ANDA218798

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Active Ingredients

Ingredient	Strength
Rilpivirine Hydrochloride	25 mg/1

Drug Class

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

Packaging Options(1)

70069-0848-30

30 TABLET, FILM COATED in 1 BOTTLE (70069-848-30)

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