Register entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- United States
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Cytovance Biologics, Inc. | 800 Research Parkway, Oklahoma City, Oklahoma (OK) 73104, United States (USA) | Analytical testing, Active ingredient (API) manufacture | 3006341547136970527 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Teriparatide | injection, solution | 83855-066DRUG FOR FURTHER PROCESSING |
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
- Health Department, Oklahoma StateOklahoma City, OK
- PD-Rx Pharmaceuticals Inc.Oklahoma City, OK
- Spaus Inc.Oklahoma City, OK
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Enquiry
Common questions
- Is Cytovance Biologics, Inc. FDA approved?
- Cytovance Biologics, 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 Cytovance Biologics, Inc.'s drugs manufactured?
- The FDA register lists Oklahoma City, OK. Registered operations: analytical testing, active ingredient (API) manufacture.
- What drugs does Cytovance Biologics, Inc. make?
- 1 product is listed under Cytovance Biologics, Inc. in the openFDA NDC Directory, most often as injection, 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.