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
- 59651-679_2db1a899-f115-4da5-89fe-6e5b41086f6c
- Product NDC
- 59651-679
- Form
- TABLET, FILM COATED
- Composition / generic term
- Bisoprolol Fumarate and Hydrochlorothiazide
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260121
- Source listing expiry
- 20271231
Source-listed ingredients
- BISOPROLOL FUMARATE — 5 mg/1
- HYDROCHLOROTHIAZIDE — 6.25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (59651-679-01) · 59651-679-01
- 500 TABLET, FILM COATED in 1 BOTTLE (59651-679-05) · 59651-679-05
- 30 TABLET, FILM COATED in 1 BOTTLE (59651-679-30) · 59651-679-30
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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