# Valsartan and Hydrochlorothiazide

NDC: 68180-101
Generic name: Valsartan and Hydrochlorothiazide
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20130321

FDA application: ANDA078946

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1
- VALSARTAN: 320 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68180-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d74a85de-5917-401a-b92d-6a95da5d30a6