# candesartan cilexetil and hydrochlorothiazide

NDC: 70771-1327
Generic name: candesartan cilexetil and hydrochlorothiazide
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180414

FDA application: ANDA203466

## Active ingredients

- CANDESARTAN CILEXETIL: 32 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:"70771-1327"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1327
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb328bc1-5738-4620-b2b3-442e98388a86