# Hydrochlorothiazide

NDC: 55700-006
Generic name: Hydrochlorothiazide
Labeler / Manufacturer: Lake Erie Medical DBA Quality Care Products LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090702
Marketing ended: 20270331
FDA application: ANDA040907

## Active ingredients

- HYDROCHLOROTHIAZIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55700-006"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-006
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9e6a0c83-1494-44ca-90e0-3f43fa8ec746