Register entry

Buchler GmbH

Data as of · How to read this entry

Registered sites
1
Active NDC listings
6
Live patents
0
Countries
1
Base
Germany
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Buchler GmbHHarxb�tteler Strasse 3, Chininfabrik Braunschweig, D-38110, Germany (DEU)Active ingredient (API) manufacture3002806608331565379
Catalogue

Drug listings by form and route

6

6 active NDC listings: 6 bulk ingredient. By marketing category: BULK INGREDIENT 6.

Dosage formNDCs
powder6
RouteNDCs
Labeller name on the listingNDCs
buchler gmbh6
Catalogue

Marketed products

6
BrandGeneric nameForm / routeNDC
-Quinic Acidpowder12065-0200BULK INGREDIENT
-Quinidine Gluconatepowder12065-1702BULK INGREDIENT
-Quinidine Sulfatepowder12065-1701BULK INGREDIENT
-Quinine Basepowder12065-1706BULK INGREDIENT
-Quinine Hydrochloridepowder12065-1703BULK INGREDIENT
-Quinine Sulfatepowder12065-1704BULK INGREDIENT
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Comparable companies in Germany

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Common questions

Is Buchler GmbH FDA approved?
Buchler 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 Buchler GmbH's drugs manufactured?
The FDA register lists Chininfabrik Braunschweig. Registered operations: active ingredient (API) manufacture.
What drugs does Buchler GmbH make?
6 products are listed under Buchler 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.