# VALSARTAN AND HYDROCHLOROTHIAZIDE

NDC: 50228-149
Generic name: valsartan and hydrochlorothiazide
Labeler / Manufacturer: ScieGen Pharmaceuticals, INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260727

FDA application: ANDA204687

## Active ingredients

- VALSARTAN: 160 mg/1
- HYDROCHLOROTHIAZIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50228-149"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50228-149
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=17362ff8-07bb-42c6-a100-8adb93be0348