# Hydrochlorothiazide

NDC: 50090-6931
Generic name: Hydrochlorothiazide
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20070312

FDA application: ANDA040707

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-6931"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-6931
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=01ad3531-5ed9-434c-b7d5-02d72aa82e46