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
- 63187-367_4efb5b48-aa05-4377-a3af-d2bb6530ab32
- Product NDC
- 63187-367
- Form
- TABLET
- Composition / generic term
- Hydrochlorothiazide
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130410
- 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 (63187-367-00) · 63187-367-00
- 3 TABLET in 1 BOTTLE (63187-367-03) · 63187-367-03
- 10 TABLET in 1 BOTTLE (63187-367-10) · 63187-367-10
- 14 TABLET in 1 BOTTLE (63187-367-14) · 63187-367-14
- 30 TABLET in 1 BOTTLE (63187-367-30) · 63187-367-30
- 60 TABLET in 1 BOTTLE (63187-367-60) · 63187-367-60
- 90 TABLET in 1 BOTTLE (63187-367-90) · 63187-367-90
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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