# Micardis HCT

NDC: 0597-0042
Generic name: telmisartan and hydrochlorothiazide
Labeler / Manufacturer: Boehringer Ingelheim Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20001201

FDA application: NDA021162

## Active ingredients

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

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0597-0042"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0597-0042
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b078dae2-664d-4144-847a-3b9d9b557402