# VALSARTAN

NDC: 51660-141
Generic name: VALSARTAN
Labeler / Manufacturer: Ohm Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20140707

FDA application: ANDA077492

## Active ingredients

- VALSARTAN: 80 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-141"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-141
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ab5e0e5a-5bdf-4cfc-9d18-57ea4d642f65