# Amiloride Hydrochloride and Hydrochlorothiazide

NDC: 0555-0483
Generic name: Amiloride Hydrochloride and Hydrochlorothiazide
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19891201

FDA application: ANDA071111

## Active ingredients

- AMILORIDE HYDROCHLORIDE: 5 mg/1
- HYDROCHLOROTHIAZIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0555-0483"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0555-0483
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8b2c581a-f955-4a8e-bf85-e768e903fd10