# Sacubitril and Valsartan

NDC: 70069-855
Generic name: Sacubitril and Valsartan
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260221

FDA application: ANDA219983

## Active ingredients

- SACUBITRIL: 97 mg/1
- VALSARTAN: 103 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-855"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-855
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f88efbb-3718-43a1-91d4-da5943ccfca1