# HYDROCHLOROTHIAZIDE

NDC: 70518-3633
Generic name: hydrochlorothiazide
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230206
Marketing ended: 20260630
FDA application: ANDA085182

## 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:"70518-3633"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3633
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db1213f0-a981-4d30-86b3-372e4dadc734