# Hydrochlorothiazide

NDC: 71205-419
Generic name: Hydrochlorothiazide
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20080815

FDA application: ANDA040907

## 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:"71205-419"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-419
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ff448eb4-b48f-46f5-ac30-f03aad08f9f5