# Hydrochlorothiazide

NDC: 66267-106
Generic name: Hydrochlorothiazide
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20130410

FDA application: ANDA202556

## Active ingredients

- HYDROCHLOROTHIAZIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"66267-106"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66267-106
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e35fb03-9173-6731-e054-00144ff8d46c