Register 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| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Spaus Inc. | 755 Research Parkway, Ste. 461, Oklahoma City, Oklahoma (OK) 73104, United States (USA) | Active ingredient (API) manufacture, distribute, Finished drug manufacture | 3015301379080858349 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| TRIHERBAL | Arnica montana, Phytolacca decandra, Sanguinaria canadensis | capsule, oral | 71989-718UNAPPROVED HOMEOPATHIC |
Neighbours
Registered in the same town
6- ACA Management, LLCOklahoma City, OK
- Anesthesia Service, Inc.Oklahoma City, OK
- Carts and Parts INC.Oklahoma City, OK
- Cytovance Biologics, Inc.Oklahoma City, OK
- Health Department, Oklahoma StateOklahoma City, OK
- PD-Rx Pharmaceuticals Inc.Oklahoma City, OK
Compare
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- Newton Laboratories, Inc.1 site · 271 NDC
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.