United States · FDA National Drug Code directory
BISOPROLOL FUMARATE
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
- 70095-020_6ce4dc4f-ad08-424e-b90d-400de0b7050a
- Product NDC
- 70095-020
- Form
- TABLET, FILM COATED
- Composition / generic term
- BISOPROLOL FUMARATE
- Labeler
- Sun Pharmaceutical Industries Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240310
- Source listing expiry
- 20261231
Source-listed ingredients
- BISOPROLOL FUMARATE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE, UNIT-DOSE (70095-020-01) · 70095-020-01
- 100 TABLET, FILM COATED in 1 BOTTLE (70095-020-02) · 70095-020-02
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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