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
- 82804-972_4c1a2fb9-133d-4bd5-a336-e47d54f22c97
- Product NDC
- 82804-972
- Form
- TABLET
- Composition / generic term
- Hydrochlorothiazide
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200925
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCHLOROTHIAZIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (82804-972-00) · 82804-972-00
- 1000 TABLET in 1 BOTTLE (82804-972-11) · 82804-972-11
- 30 TABLET in 1 BOTTLE (82804-972-30) · 82804-972-30
- 500 TABLET in 1 BOTTLE (82804-972-55) · 82804-972-55
- 60 TABLET in 1 BOTTLE (82804-972-60) · 82804-972-60
- 120 TABLET in 1 BOTTLE (82804-972-72) · 82804-972-72
- 90 TABLET in 1 BOTTLE (82804-972-90) · 82804-972-90
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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