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
- 69584-362_a86b0c8b-1ae7-4bfc-a236-c3d7fdd8959c
- Product NDC
- 69584-362
- Form
- TABLET
- Composition / generic term
- Hydrochlorothiazide
- Labeler
- Oxford Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200925
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCHLOROTHIAZIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (69584-362-10) · 69584-362-10
- 1000 TABLET in 1 BOTTLE (69584-362-90) · 69584-362-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →