# Hydrochlorothiazide

NDC: 68645-510
Generic name: Hydrochlorothiazide
Labeler / Manufacturer: Legacy Pharmaceutical Packaging, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19730112

FDA application: ANDA083177

## 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:"68645-510"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68645-510
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d6ea4b4-1e3c-4f3f-989c-1a3a3c0da6bd