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
0378-0505_05ad15d0-4472-45a9-8dd6-fc5d13c2a858
Product NDC
0378-0505
Form
TABLET, FILM COATED
Composition / generic term
bisoprolol fumarate and hydrochlorothiazide
Labeler
Mylan Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20210222
Source listing expiry
20271231

Source-listed ingredients

  • BISOPROLOL FUMARATE — 10 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, PLASTIC (0378-0505-01) · 0378-0505-01

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 →