Drug

Who makes bisoprolol fumarate and hydrochlorothiazide?

12 companies list bisoprolol fumarate and hydrochlorothiazide as a human prescription drug. Forms: tablet; tablet, film coated. Routes: oral.

Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology

Companies listing bisoprolol fumarate and hydrochlorothiazide

CompanyFormsApplicationNDCsRegistered sites
International Medication Systems, Ltd.United Statestablet; tablet, film coatedANDA, NDA AUTHORIZED GENERICANDA212678, ANDA215562, ANDA21599563
Bryant Ranch PrepackUnited Statestablet; tablet, film coatedANDAANDA079106, ANDA212678, ANDA21599561
Zydus Lifesciences LimitedIndiatablet, film coatedANDAANDA215666312
Glenmark Pharmaceuticals Inc., USAIndiatablet, film coatedANDAANDA21599539
Aurobindo Pharma LimitedIndiatablet, film coatedANDAANDA21792236
Unichem Laboratories Limited, IndiaIndiatabletANDAANDA07910635
ANI Pharmaceuticals, Inc.United StatestabletANDAANDA21556231
Marlex Pharmaceuticals, IncUnited StatestabletANDAANDA21556231
Edenbridge Pharmaceuticals LLC.tablet, film coatedANDAANDA21267830
Mylan Pharmaceuticals, Inc.tablet, film coatedANDAANDA07576830
Viona Pharmaceuticals Inc.tablet, film coatedANDAANDA21566630
Teva Pharmaceutical Industries Ltd.Canadatablet, film coatedNDA AUTHORIZED GENERICNDA02018616
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Common questions

Who makes bisoprolol fumarate and hydrochlorothiazide?
12 companies list bisoprolol fumarate and hydrochlorothiazide as a human prescription drug in the openFDA NDC Directory, led by International Medication Systems, Ltd., Bryant Ranch Prepack, Zydus Lifesciences Limited, Glenmark Pharmaceuticals Inc., USA, Aurobindo Pharma Limited. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
Is there a generic bisoprolol fumarate and hydrochlorothiazide?
11 companies list bisoprolol fumarate and hydrochlorothiazide under an abbreviated new drug application (ANDA), the application type used for generics. Listing status is from the NDC Directory; it is not a statement of availability.