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
72888-092_43603823-594f-cbe7-e063-6294a90a9153
Product NDC
72888-092
Form
TABLET, FILM COATED
Composition / generic term
Bisoprolol Fumarate
Labeler
Advagen Pharma Ltd
Marketing category
ANDA
Marketing start / end (source format)
20001116
Source listing expiry
20261231

Source-listed ingredients

  • BISOPROLOL FUMARATE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET, FILM COATED in 1 BOTTLE (72888-092-00) · 72888-092-00
  • 100 TABLET, FILM COATED in 1 BOTTLE (72888-092-01) · 72888-092-01
  • 500 TABLET, FILM COATED in 1 BOTTLE (72888-092-05) · 72888-092-05
  • 30 TABLET, FILM COATED in 1 BOTTLE (72888-092-30) · 72888-092-30

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 →