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
- 69367-219_9fe99531-f04b-447d-bc2b-61177b064d9e
- Product NDC
- 69367-219
- Form
- CAPSULE
- Composition / generic term
- Hydrochlorothiazide
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190607
- Source listing expiry
- 20271231
Source-listed ingredients
- HYDROCHLOROTHIAZIDE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-01) · 69367-219-01
- 500 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-05) · 69367-219-05
- 1000 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-10) · 69367-219-10
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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