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Data / Drug companies / Avyxa Pharma, LLC

Avyxa Pharma, LLC: 31 products in the FDA NDC directory, labeler code 83831

Avyxa Pharma, LLC (labeler code 83831) lists 31 products in the FDA National Drug Code Directory, covering 15 finished drugs by generic name. By type: 31 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on October 29, 2026.

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
83831
Products in commercial distribution
31
Packages
31
Finished drugs by generic name
15
Prescription products
31
Over the counter products
0
Flagged as original packager
24 of 24 products that carry the flag
Started marketing in the last 12 months
12
Earliest marketing start
May 9, 2024
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)31100%

Products by type

TypeProductsShare
Prescription drugs31100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Injection1548.4%
Injection, solution1032.3%
Injection, powder, lyophilized, for solution516.1%
Kit13.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Axycis83831-158Injection, solutionNew drug applications (NDA)October 29, 2026
Gobarden83831-176Injection, solutionNew drug applications (NDA)September 25, 2026
Avopef83831-145InjectionNew drug applications (NDA)September 14, 2026
Navitrux83831-153Injection, powder, lyophilized, for solutionNew drug applications (NDA)July 23, 2026
Favlyxa83831-164Injection, solutionNew drug applications (NDA)July 15, 2026
Cligavyx83831-159InjectionNew drug applications (NDA)July 1, 2026
Bendamustine hydrochloride83831-183InjectionNew drug applications (NDA)May 29, 2026
Avopef83831-144InjectionNew drug applications (NDA)April 1, 2026
Favlyxa83831-143Injection, solutionNew drug applications (NDA)April 1, 2026
Vykoura83831-149InjectionNew drug applications (NDA)March 16, 2026
Vykoura83831-148InjectionNew drug applications (NDA)March 16, 2026
Vykoura83831-147InjectionNew drug applications (NDA)March 16, 2026
Kyxata83831-142InjectionNew drug applications (NDA)September 10, 2025
Kyxata83831-141InjectionNew drug applications (NDA)September 10, 2025
Avgemsi83831-124Injection, solutionNew drug applications (NDA)August 3, 2025
Avgemsi83831-123Injection, solutionNew drug applications (NDA)August 3, 2025
Lutrate depot83831-134KitNew drug applications (NDA)March 26, 2025
Frindovyx83831-121InjectionNew drug applications (NDA)March 19, 2025
Frindovyx83831-120InjectionNew drug applications (NDA)March 19, 2025
Frindovyx83831-119InjectionNew drug applications (NDA)March 19, 2025
Axtle83831-132Injection, powder, lyophilized, for solutionNew drug applications (NDA)January 1, 2025
Axtle83831-131Injection, powder, lyophilized, for solutionNew drug applications (NDA)January 1, 2025
Pemetrexed dipotassium83831-112Injection, powder, lyophilized, for solutionNew drug applications (NDA)January 1, 2025
Pemetrexed dipotassium83831-111Injection, powder, lyophilized, for solutionNew drug applications (NDA)January 1, 2025
Posfrea83831-105Injection, solutionNew drug applications (NDA)September 30, 2024

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.