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Data / Drug companies / Tigecycline

Tigecycline: 6 companies and 8 products in the FDA NDC directory

Tigecycline is listed in the FDA National Drug Code Directory by 6 companies, with 8 products in commercial distribution. 5 of the products (62.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, powder, lyophilized, for solution, and the newest product started marketing on April 1, 2026.

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Companies listing it
6
Products
8
Generic (ANDA) products
5 (62.5%)
Application numbers
6
Routes
Intravenous, Parenteral
Brand names
Tygacil
openFDA record search
api.fda.gov

Companies that list tigecycline

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Meitheal Pharmaceuticals Inc.2injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 1, 2026
Wyeth Pharmaceuticals LLC, a Subsidiary of Pfizer Inc.2injection, powder, lyophilized, for solutionNew drug applications (NDA)February 8, 2017
Amneal Pharmaceuticals LLC1injection, powder, lyophilized, for solutionNew drug applications (NDA)January 31, 2018
Apotex Corp.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 9, 2019
Eugia US LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 11, 2019
Sandoz Inc1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)November 30, 2017

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for solution8100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)562.5%
New drug applications (NDA)337.5%

Pharmacologic classes

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.