Register entry

Spaus 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) manufacture1distribute1Finished drug manufacture1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Spaus Inc.755 Research Parkway, Ste. 461, Oklahoma City, Oklahoma (OK) 73104, United States (USA)Active ingredient (API) manufacture, distribute, Finished drug manufacture3015301379080858349
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
TRIHERBALArnica montana, Phytolacca decandra, Sanguinaria canadensiscapsule, oral71989-718UNAPPROVED HOMEOPATHIC
Neighbours

Registered in the same town

6
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Comparable companies in United States

Enquiry

Common questions

Is Spaus Inc. FDA approved?
Spaus 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 Spaus Inc.'s drugs manufactured?
The FDA register lists Oklahoma City, OK. Registered operations: active ingredient (API) manufacture, distribute, finished drug manufacture.
What drugs does Spaus Inc. make?
1 product is listed under Spaus Inc. in the openFDA NDC Directory, most often as capsule. 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.