# Hydrochlorothiazide

NDC: 51655-502
Generic name: Hydrochlorothiazide
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150306

FDA application: ANDA202556

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-502"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-502
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=57a2f9bd-8ca5-437e-b911-5207f94cc6ba