Register entry

Arevipharma GmbH

Data as of · How to read this entry

Registered sites
1
Active NDC listings
13
Live patents
0
Countries
1
Base
Germany
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Arevipharma GmbHMeisner Str 35, Radebeul, 01445, Germany (DEU)Active ingredient (API) manufacture1000505976333166114
Catalogue

Drug listings by form and route

13

13 active NDC listings: 13 bulk ingredient. By marketing category: BULK INGREDIENT 13.

Dosage formNDCs
powder13
RouteNDCs
Labeller name on the listingNDCs
arevipharma gmbh13
Catalogue

Marketed products

13
BrandGeneric nameForm / routeNDC
-Arketamine Hydrochloridepowder10920-701BULK INGREDIENT
-Bisoprolol fumaratepowder10920-571BULK INGREDIENT
-Buprenorphinepowder10920-593BULK INGREDIENT
-Buprenorphine hydrochloridepowder10920-590BULK INGREDIENT
-Diethylpropion Hydrochloridepowder10920-600BULK INGREDIENT
-Dimethyl Fumaratepowder10920-598BULK INGREDIENT
-Doxapram hydrochloride monohydratepowder10920-601BULK INGREDIENT
-Esketamine Hydrochloridepowder10920-700BULK INGREDIENT
-Imepitoinpowder10920-582BULK INGREDIENT
-Ketamine Hydrochloridepowder10920-597BULK INGREDIENT
-Naltrexonepowder10920-702BULK INGREDIENT
-Naltrexone hydrochloridepowder10920-704BULK INGREDIENT
-Remifentanil Hydrochloridepowder10920-703BULK INGREDIENT
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Comparable companies in Germany

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Common questions

Is Arevipharma GmbH FDA approved?
Arevipharma GmbH holds 1 FDA-registered establishment in Germany. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Arevipharma GmbH's drugs manufactured?
The FDA register lists Radebeul. Registered operations: active ingredient (API) manufacture.
What drugs does Arevipharma GmbH make?
13 products are listed under Arevipharma GmbH in the openFDA NDC Directory, most often as powder. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.