# Hydrochlorothiazide

NDC: 65862-113
Generic name: Hydrochlorothiazide
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20070919

FDA application: ANDA078164

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-113"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-113
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e31bd548-29ae-419a-831a-80ebb26e042f