# Amiloride Hydrochloride

NDC: 42794-005
Generic name: Amiloride Hydrochloride
Labeler / Manufacturer: Sigmapharm Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210614

FDA application: ANDA079133

## Active ingredients

- AMILORIDE HYDROCHLORIDE ANHYDROUS: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42794-005"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42794-005
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de12b6f3-3791-4d78-90e6-c487cf951738