Register entry

Garonit Pharmaceutical, Inc.

Data as of · How to read this entry

Registered sites
1
Active NDC listings
1
Live patents
0
Countries
1
Base
United States
Authorisation

Registered operations

Active ingredient (API) manufacture1Relabelling1Repackaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Garonit Pharmaceutical, Inc.10 Madison Road, Suite A, Fairfield, New Jersey (NJ) 07004, United States (USA)Active ingredient (API) manufacture, Relabelling, Repackaging3003961853800875106
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
-CHLORHEXIDINE GLUCONATEsolution85518-020DRUG FOR FURTHER PROCESSING
Neighbours

Registered in the same town

7
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Comparable companies in United States

Enquiry

Common questions

Is Garonit Pharmaceutical, Inc. FDA approved?
Garonit Pharmaceutical, Inc. holds 1 FDA-registered establishment in the United States. 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 Garonit Pharmaceutical, Inc.'s drugs manufactured?
The FDA register lists Fairfield, NJ. Registered operations: active ingredient (API) manufacture, relabelling, repackaging.
What drugs does Garonit Pharmaceutical, Inc. make?
1 product is listed under Garonit Pharmaceutical, Inc. in the openFDA NDC Directory, most often as solution. 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.