# Rilpivirine

NDC: 70069-848
Generic name: Rilpivirine
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260130

FDA application: ANDA218798

## Active ingredients

- RILPIVIRINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-848"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-848
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fb109de9-d88d-4405-8dd6-d458cbc387d1