United States · FDA National Drug Code directory
bisoprolol fumarate and 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
- 71335-0595_83e47e72-5cf3-4db5-902e-20d7d9595cb9
- Product NDC
- 71335-0595
- Form
- TABLET
- Composition / generic term
- bisoprolol fumarate and hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101012
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCHLOROTHIAZIDE — 6.25 mg/1
- BISOPROLOL FUMARATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE, PLASTIC (71335-0595-1) · 71335-0595-1
- 90 TABLET in 1 BOTTLE, PLASTIC (71335-0595-2) · 71335-0595-2
- 28 TABLET in 1 BOTTLE, PLASTIC (71335-0595-3) · 71335-0595-3
- 100 TABLET in 1 BOTTLE, PLASTIC (71335-0595-4) · 71335-0595-4
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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