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Data / Drug companies / Eton Pharmaceuticals, Inc.

Eton Pharmaceuticals, Inc.: 15 products in the FDA NDC directory, labeler code 71863

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

Eton Pharmaceuticals, Inc. (labeler code 71863) lists 15 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 15 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on September 26, 2026.

The request: Watch Eton Pharmaceuticals, Inc. (FDA labeler code 71863): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
71863
Products in commercial distribution
15
Packages
17
Finished drugs by generic name
8
Prescription products
15
Over the counter products
0
Flagged as original packager
13 of 13 products that carry the flag
Started marketing in the last 12 months
3
Earliest marketing start
September 29, 2020
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)853.3%
Generic drugs (ANDA)640%
Biologics (BLA)16.7%

Products by type

TypeProductsShare
Prescription drugs15100%

Drugs it lists

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

DrugProductsCompanies listing it
Hydrocortisone5171
Nitisinone46
Desmopressin acetate oral solution11
Propranolol hydrochloride151
Mecasermin12
Betaine anhydrous11
Miltefosine12
Carglumic acid14

Dosage forms

Dosage formProductsShare
Capsule533.3%
Granule426.7%
Solution320%
Injection16.7%
Powder, for solution16.7%
Tablet, for suspension16.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Impavido71863-135CapsuleNew drug applications (NDA)September 26, 2026
Hemangeol71863-132SolutionNew drug applications (NDA)April 16, 2026
Desmoda71863-123SolutionNew drug applications (NDA)March 2, 2026
Khindivi71863-116SolutionNew drug applications (NDA)June 2, 2025
Increlex71863-216InjectionBiologics (BLA)April 16, 2025
Nitisinone71863-122CapsuleGeneric drugs (ANDA)January 15, 2024
Nitisinone71863-121CapsuleGeneric drugs (ANDA)January 15, 2024
Nitisinone71863-120CapsuleGeneric drugs (ANDA)January 15, 2024
Nitisinone71863-119CapsuleGeneric drugs (ANDA)January 15, 2024
Betaine Anhydrous71863-115Powder, for solutionGeneric drugs (ANDA)January 28, 2022
Carglumic Acid71863-114Tablet, for suspensionGeneric drugs (ANDA)December 20, 2021
Alkindi Sprinkle71863-112GranuleNew drug applications (NDA)September 29, 2020
Alkindi Sprinkle71863-111GranuleNew drug applications (NDA)September 29, 2020
Alkindi Sprinkle71863-110GranuleNew drug applications (NDA)September 29, 2020
Alkindi Sprinkle71863-109GranuleNew drug applications (NDA)September 29, 2020

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.