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Data / Drug companies / Insulin human

Insulin human: 4 companies and 16 products in the FDA NDC directory

Insulin human is listed in the FDA National Drug Code Directory by 4 companies, with 16 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, solution; injection, suspension; kit, and the newest product started marketing on June 1, 2025.

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
4
Products
16
Generic (ANDA) products
0 (0.0%)
Application numbers
5
Routes
Respiratory (inhalation), Subcutaneous, Parenteral, Intravenous
Brand names
Afrezza, Humulin N, Humulin R, Humulin 70/30 KwikPen, Humulin R, Humulin R U-500 KwikPen, Humulin 70/30, Myxredlin
openFDA record search
api.fda.gov

Companies that list insulin human

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Eli Lilly and Company7injection, suspension; injection, solutionBiologics (BLA)December 29, 2015
Mannkind Corporation7kit; powder, meteredBiologics (BLA)June 1, 2025
A-S Medication Solutions1injection, solutionBiologics (BLA)June 27, 1983
Baxter Healthcare Corporation1injection, solutionBiologics (BLA)July 12, 2019

Dosage forms

Dosage formProductsShare
Injection, solution531.2%
Injection, suspension425%
Kit425%
Powder, metered318.8%

Marketing categories

Marketing categoryProductsShare
Biologics (BLA)16100%

Pharmacologic classes

ClassProducts
Insulin12

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.