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Data / Drug companies / Euroapi Hungary Ltd.

Euroapi Hungary Ltd.: 17 products in the FDA NDC directory, labeler code 82231

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

Euroapi Hungary Ltd. (labeler code 82231) lists 17 products in the FDA National Drug Code Directory. By type: 17 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on February 1, 2026.

The request: Watch Euroapi Hungary Ltd. (FDA labeler code 82231): 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
82231
Products in commercial distribution
17
Packages
17
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
1
Earliest marketing start
June 6, 1989
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients17100%

Products by type

TypeProductsShare
Bulk ingredients17100%

Dosage forms

Dosage formProductsShare
Powder1376.5%
Oil423.5%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Ncx 47082231-118OilBulk ingredientsFebruary 1, 2026
Cloprostenol sodium82231-117PowderBulk ingredientsJune 6, 2025
Olmesartan medoxomil82231-116PowderBulk ingredientsOctober 18, 2023
Carboprost tromethamine82231-103PowderBulk ingredientsJanuary 17, 2022
Fexinidazole82231-107PowderBulk ingredientsJanuary 1, 2021
Travoprost82231-114OilBulk ingredientsAugust 11, 2020
Treprostinil sodium82231-115PowderBulk ingredientsNovember 28, 2019
Latanoprostene bunod82231-112OilBulk ingredientsOctober 1, 2018
Iloprost82231-109PowderBulk ingredientsSeptember 28, 2018
Hydroxychloroquine sulfate82231-108PowderBulk ingredientsAugust 31, 2018
Bimatoprost82231-102PowderBulk ingredientsMarch 7, 2018
Epoprostenol sodium82231-106PowderBulk ingredientsOctober 28, 2014
Dinoprostone82231-104PowderBulk ingredientsOctober 28, 2014
Alprostadil82231-101PowderBulk ingredientsOctober 28, 2014
Latanoprost82231-111OilBulk ingredientsJanuary 1, 2013
Irbesartan82231-110PowderBulk ingredientsJune 17, 2009
Selegiline hydrochloride82231-113PowderBulk ingredientsJune 6, 1989

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.