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
- 71335-0269_ca065153-d3c4-4342-b690-01177484e06e
- Product NDC
- 71335-0269
- Form
- TABLET
- Composition / generic term
- Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130410
- Source listing expiry
- 20271231
Source-listed ingredients
- HYDROCHLOROTHIAZIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE (71335-0269-0) · 71335-0269-0
- 100 TABLET in 1 BOTTLE (71335-0269-1) · 71335-0269-1
- 30 TABLET in 1 BOTTLE (71335-0269-2) · 71335-0269-2
- 7 TABLET in 1 BOTTLE (71335-0269-3) · 71335-0269-3
- 14 TABLET in 1 BOTTLE (71335-0269-4) · 71335-0269-4
- 60 TABLET in 1 BOTTLE (71335-0269-5) · 71335-0269-5
- 2 TABLET in 1 BOTTLE (71335-0269-6) · 71335-0269-6
- 90 TABLET in 1 BOTTLE (71335-0269-7) · 71335-0269-7
- 4 TABLET in 1 BOTTLE (71335-0269-8) · 71335-0269-8
- 8 TABLET in 1 BOTTLE (71335-0269-9) · 71335-0269-9
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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