Is F. Hunziker + Co AG FDA approved?

F. Hunziker + Co AG holds 1 FDA-registered establishment in Switzerland. 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.

What drugs does F. Hunziker + Co AG make?

4 products are listed under F. Hunziker + Co AG in the openFDA NDC Directory, most often as pastille. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

F. Hunziker + Co AG

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 4
Live patents: 0
Countries: 1
Base: Switzerland

Authorisation

Registered operations

Active ingredient (API) manufacture1Finished drug manufacture1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
F. Hunziker + Co AG	Heimstrasse 18, Dietikon, Switzerland 8953, Switzerland (CHE)	Active ingredient (API) manufacture, Finished drug manufacture	3008605156480128933

Catalogue

Drug listings by form and route

4 active NDC listings: 4 drug for further processing. By marketing category: DRUG FOR FURTHER PROCESSING 4.

Dosage form	NDCs
pastille	4

Route	NDCs

Labeller name on the listing	NDCs
f. hunziker + co ag	4

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	ORNITHOGALUM UMBELLATUM, PRUNUS CERASIFERA, CLEMATIS VITALBA, HELIANTHEMUM NUMMULARIUM, IMPATIENS GLANDULIFERA	pastille	85353-000DRUG FOR FURTHER PROCESSING
-	ORNITHOGALUM UMBELLATUM, PRUNUS CERASIFERA, CLEMATIS VITALBA, HELIANTHEMUM NUMMULARIUM, IMPATIENS GLANDULIFERA	pastille	85353-001DRUG FOR FURTHER PROCESSING
-	ORNITHOGALUM UMBELLATUM, PRUNUS CERASIFERA, CLEMATIS VITALBA, HELIANTHEMUM NUMMULARIUM, IMPATIENS GLANDULIFERA	pastille	85353-002DRUG FOR FURTHER PROCESSING
-	ORNITHOGALUM UMBELLATUM, PRUNUS CERASIFERA, CLEMATIS VITALBA, HELIANTHEMUM NUMMULARIUM, IMPATIENS GLANDULIFERA	pastille	85353-003DRUG FOR FURTHER PROCESSING

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Enquiry

Common questions

Is F. Hunziker + Co AG FDA approved?: F. Hunziker + Co AG holds 1 FDA-registered establishment in Switzerland. 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 F. Hunziker + Co AG's drugs manufactured?: The FDA register lists Dietikon. Registered operations: active ingredient (API) manufacture, finished drug manufacture.
What drugs does F. Hunziker + Co AG make?: 4 products are listed under F. Hunziker + Co AG in the openFDA NDC Directory, most often as pastille. 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.