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Data / Drug companies / Antares Pharma, Inc.

Antares Pharma, Inc.: 10 products in the FDA NDC directory, labeler code 54436

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

Antares Pharma, Inc. (labeler code 54436) lists 10 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 10 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on November 15, 2018.

The request: Watch Antares Pharma, Inc. (FDA labeler code 54436): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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.

Labeler code
54436
Products in commercial distribution
10
Packages
29
Finished drugs by generic name
2
Prescription products
10
Over the counter products
0
Controlled substance products
Schedule III 3
Flagged as original packager
10 of 10 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
7
Earliest marketing start
October 11, 2013
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)10100%

Products by type

TypeProductsShare
Prescription drugs10100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Methotrexate731
Testosterone enanthate33

Dosage forms

Dosage formProductsShare
Injection, solution770%
Injection330%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Xyosted54436-275InjectionNew drug applications (NDA)November 15, 2018
Xyosted54436-250InjectionNew drug applications (NDA)November 15, 2018
Xyosted54436-200InjectionNew drug applications (NDA)November 15, 2018
Otrexup54436-025Injection, solutionNew drug applications (NDA)October 11, 2013
Otrexup54436-022Injection, solutionNew drug applications (NDA)October 11, 2013
Otrexup54436-020Injection, solutionNew drug applications (NDA)October 11, 2013
Otrexup54436-017Injection, solutionNew drug applications (NDA)October 11, 2013
Otrexup54436-015Injection, solutionNew drug applications (NDA)October 11, 2013
Otrexup54436-012Injection, solutionNew drug applications (NDA)October 11, 2013
Otrexup54436-010Injection, solutionNew drug applications (NDA)October 11, 2013

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.