United States · FDA National Drug Code directory
Bisoprolol
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
- 52817-271_2a9e4180-cb1c-f924-e063-6394a90a60c6
- Product NDC
- 52817-271
- Form
- TABLET, FILM COATED
- Composition / generic term
- Bisoprolol fumarate
- Labeler
- TruPharma, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190620
- Source listing expiry
- 20261231
Source-listed ingredients
- BISOPROLOL FUMARATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (52817-271-10) · 52817-271-10
- 30 TABLET, FILM COATED in 1 BOTTLE (52817-271-30) · 52817-271-30
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 →