# telmisartan and hydrochlorothiazide

NDC: 70756-317
Generic name: telmisartan and hydrochlorothiazide
Labeler / Manufacturer: Lifestar Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20251225

FDA application: ANDA218406

## Active ingredients

- HYDROCHLOROTHIAZIDE: 25 mg/1
- TELMISARTAN: 80 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70756-317"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70756-317
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0c1bd0f4-034e-486c-ae46-2855c8c9ebda