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Data / Drug companies / Triazolam

Triazolam: 9 companies and 14 products in the FDA NDC directory

Triazolam is listed in the FDA National Drug Code Directory by 9 companies, with 14 products in commercial distribution. 11 of the products (78.6%) 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 December 30, 2022.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
9
Products
14
Generic (ANDA) products
11 (78.6%)
Application numbers
3
Controlled substance schedule
Schedule IV
Routes
Oral
openFDA record search
api.fda.gov

Companies that list triazolam

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions2tabletGeneric drugs (ANDA)December 30, 2022
Ingenus Pharmaceuticals, LLC2tabletGeneric drugs (ANDA)October 20, 2020
Mylan Pharmaceuticals Inc.2tabletAuthorized generics (NDA)November 15, 1982
Zydus Lifesciences Limited2tabletGeneric drugs (ANDA)December 30, 2022
Zydus Pharmaceuticals USA Inc.2tabletGeneric drugs (ANDA)December 30, 2022
Aphena Pharma Solutions - Tennessee, LLC1tabletAuthorized generics (NDA)November 15, 1982
Bryant Ranch Prepack1tabletGeneric drugs (ANDA)October 20, 2020
PD-Rx Pharmaceuticals, Inc.1tabletGeneric drugs (ANDA)October 20, 2020
Proficient Rx LP1tabletGeneric drugs (ANDA)October 20, 2020

Dosage forms

Dosage formProductsShare
Tablet14100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1178.6%
Authorized generics (NDA)321.4%

Pharmacologic classes

ClassProducts
Benzodiazepine14

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