# Hydrochlorothiazide

NDC: 69584-362
Generic name: Hydrochlorothiazide
Labeler / Manufacturer: Oxford Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200925

FDA application: ANDA087068

## Active ingredients

- HYDROCHLOROTHIAZIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69584-362"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69584-362
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=afbb9a0e-c22f-4133-8015-b4b2ab4d32e6