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
68462-879_6154a348-821d-46cc-a830-ac5684f9525a
Product NDC
68462-879
Form
TABLET, FILM COATED
Composition / generic term
Bisoprolol Fumarate and Hydrochlorothiazide
Labeler
GLENMARK PHARMACEUTICALS INC., USA
Marketing category
ANDA
Marketing start / end (source format)
20220126
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 (68462-879-01) · 68462-879-01
  • 500 TABLET, FILM COATED in 1 BOTTLE (68462-879-05) · 68462-879-05
  • 30 TABLET, FILM COATED in 1 BOTTLE (68462-879-30) · 68462-879-30

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.

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Bisoprolol Fumarate and Hydrochlorothiazide — United States | Molindra Medicines