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Data / Drug companies / Arevipharma GmbH

Arevipharma GmbH: 13 products in the FDA NDC directory, labeler code 10920

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

Arevipharma GmbH (labeler code 10920) lists 13 products in the FDA National Drug Code Directory. By type: 13 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on August 18, 2026.

The request: Watch Arevipharma GmbH (FDA labeler code 10920): 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
10920
Products in commercial distribution
13
Packages
31
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule II 1, Schedule III 5, Schedule IV 1
Started marketing in the last 12 months
2
Earliest marketing start
November 23, 2010
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients13100%

Products by type

TypeProductsShare
Bulk ingredients13100%

Dosage forms

Dosage formProductsShare
Powder13100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Naltrexone hydrochloride10920-704PowderBulk ingredientsAugust 18, 2026
Remifentanil hydrochloride10920-703PowderBulk ingredientsMay 28, 2026
Naltrexone10920-702PowderBulk ingredientsFebruary 3, 2025
Arketamine hydrochloride10920-701PowderBulk ingredientsJanuary 13, 2022
Esketamine hydrochloride10920-700PowderBulk ingredientsJanuary 12, 2022
Doxapram hydrochloride monohydrate10920-601PowderBulk ingredientsOctober 25, 2017
Diethylpropion hydrochloride10920-600PowderBulk ingredientsMay 12, 2014
Dimethyl fumarate10920-598PowderBulk ingredientsDecember 17, 2013
Ketamine hydrochloride10920-597PowderBulk ingredientsDecember 9, 2013
Buprenorphine10920-593PowderBulk ingredientsJuly 30, 2012
Buprenorphine hydrochloride10920-590PowderBulk ingredientsMarch 2, 2011
Imepitoin10920-582PowderBulk ingredientsJanuary 11, 2011
Bisoprolol fumarate10920-571PowderBulk ingredientsNovember 23, 2010

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.