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
- 71205-419_57d5edff-ebf7-4a58-aa93-78213250d248
- Product NDC
- 71205-419
- Form
- TABLET
- Composition / generic term
- Hydrochlorothiazide
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080815
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCHLOROTHIAZIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET in 1 BOTTLE (71205-419-14) · 71205-419-14
- 30 TABLET in 1 BOTTLE (71205-419-30) · 71205-419-30
- 60 TABLET in 1 BOTTLE (71205-419-60) · 71205-419-60
- 90 TABLET in 1 BOTTLE (71205-419-90) · 71205-419-90
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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