United States · FDA National Drug Code directory

Amiloride Hydrochloride and Hydrochlorothiazide

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 0555-0483_3c6d3a11-6d0b-4109-89cd-658827847fea
Product NDC: 0555-0483
Form: TABLET
Composition / generic term: Amiloride Hydrochloride and Hydrochlorothiazide
Labeler: Teva Pharmaceuticals USA, Inc.
Marketing category: ANDA
Marketing start / end (source format): 19891201
Source listing expiry: 20261231

Source-listed ingredients

AMILORIDE HYDROCHLORIDE — 5 mg/1
HYDROCHLOROTHIAZIDE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET in 1 BOTTLE (0555-0483-02) · 0555-0483-02
1000 TABLET in 1 BOTTLE (0555-0483-05) · 0555-0483-05

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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