United States · FDA National Drug Code directory
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
- 43547-398_d8ce29b2-7f3a-4944-bf9e-0fcebb25d3c4
- Product NDC
- 43547-398
- Form
- TABLET
- Composition / generic term
- Hydrochlorothiazide
- Labeler
- Solco Healthcare U.S., LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020329
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCHLOROTHIAZIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE, PLASTIC (43547-398-01) · 43547-398-01
- 30 TABLET in 1 BOTTLE, PLASTIC (43547-398-03) · 43547-398-03
- 50 TABLET in 1 BOTTLE, PLASTIC (43547-398-05) · 43547-398-05
- 100 TABLET in 1 BOTTLE, PLASTIC (43547-398-10) · 43547-398-10
- 1000 TABLET in 1 BOTTLE, PLASTIC (43547-398-11) · 43547-398-11
- 500 TABLET in 1 BOTTLE, PLASTIC (43547-398-50) · 43547-398-50
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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