# Hydrochlorothiazide

NDC: 68071-2411
Generic name: Hydrochlorothiazide
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20130410

FDA application: ANDA202556

## Active ingredients

- HYDROCHLOROTHIAZIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-2411"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-2411
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c2db7e27-952f-c3f6-e053-2995a90af7c1