Skip to the page

Data / Drug companies / Tiotropium bromide

Tiotropium bromide: 3 companies and 4 products in the FDA NDC directory

Tiotropium bromide is listed in the FDA National Drug Code Directory by 3 companies, with 4 products in commercial distribution. 1 of the products (25.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule, and the newest product started marketing on August 16, 2023.

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
3
Products
4
Generic (ANDA) products
1 (25.0%)
Application numbers
2
Routes
Oral, Respiratory (inhalation)
Brand names
Spiriva HandiHaler
openFDA record search
api.fda.gov

Companies that list tiotropium bromide

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions2capsuleNew drug applications (NDA)October 11, 2005
Boehringer Ingelheim Pharmaceuticals, Inc.1capsuleNew drug applications (NDA)October 11, 2005
Lupin Pharmaceuticals, Inc.1capsuleGeneric drugs (ANDA)August 16, 2023

Dosage forms

Dosage formProductsShare
Capsule4100%

Marketing categories

Marketing categoryProductsShare
New drug applications (NDA)375%
Generic drugs (ANDA)125%

Pharmacologic classes

ClassProducts
Anticholinergic4

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.