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Data / Drug companies / Lisinopril and hydrochlorothiazide tablets

Lisinopril and hydrochlorothiazide tablets: 12 companies and 38 products in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Lisinopril and hydrochlorothiazide tablets is listed in the FDA National Drug Code Directory by 12 companies, with 38 products in commercial distribution. 38 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, and the newest product started marketing on November 6, 2025.

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Companies listing it
12
Products
38
Generic (ANDA) products
38 (100.0%)
Application numbers
2
Routes
Oral
Brand names
Lisinopril and Hydrochlorothiazide
openFDA record search
api.fda.gov

Companies that list lisinopril and hydrochlorothiazide tablets

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions7tabletGeneric drugs (ANDA)December 26, 2019
Bryant Ranch Prepack5tabletGeneric drugs (ANDA)December 26, 2019
Aphena Pharma Solutions - Tennessee, LLC4tabletGeneric drugs (ANDA)May 1, 2019
NuCare Pharmaceuticals,Inc.4tabletGeneric drugs (ANDA)December 26, 2019
Cipla USA Inc.3tabletGeneric drugs (ANDA)December 26, 2019
Exelan Pharmaceuticals Inc.3tabletGeneric drugs (ANDA)May 1, 2019
Preferred Pharmaceuticals Inc.3tabletGeneric drugs (ANDA)October 1, 2022
Solco Healthcare US, LLC3tabletGeneric drugs (ANDA)March 12, 2015
Remedyrepack Inc.2tabletGeneric drugs (ANDA)November 6, 2025
St. Mary's Medical Park Pharmacy2tabletGeneric drugs (ANDA)June 29, 2023
Proficient Rx LP1tabletGeneric drugs (ANDA)March 12, 2015
Proficient Rx LP1tabletGeneric drugs (ANDA)March 12, 2015

Dosage forms

Dosage formProductsShare
Tablet38100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)38100%

Pharmacologic classes

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.