Is Zoetis Inc FDA approved?

Zoetis Inc holds 11 FDA-registered establishments across 6 countries. 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 Zoetis Inc's drugs manufactured?

At registered sites in Australia, Belgium, Spain, Ireland, Italy, the United States. The FDA register lists Rutherford; Ottignies-Louvain-la-Neuve; Bianya; The Copse; Tullamore; CATANIA, and 4 more. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging, particle size reduction, relabelling, repackaging, sterilize.

What drugs does Zoetis Inc make?

29 products are listed under Zoetis Inc in the openFDA NDC Directory, most often as tablet, chewable; powder; tablet. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Zoetis Inc

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

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Registered sites: 11
Active NDC listings: 29
Live patents: 0
Countries: 6
Base: United States

Authorisation

Registered operations

Analytical testing8Active ingredient (API) manufacture6Labelling8Finished drug manufacture7Packaging9particle size reduction1Relabelling4Repackaging4sterilize3

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Jurox Pty. LimitedRegistrant: Zoetis Inc	85 Gardiner Street, Rutherford, NSW 2320, Australia (AUS)	Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging, sterilize	3003483729751438037
Zoetis Belgium S.A.Registrant: Zoetis Inc	Rue Laid Burniat 1, Ottignies-Louvain-la-Neuve, Louvain-la-Neuve B1348, Belgium (BEL)	Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging, sterilize	3010087842370053142
Zoetis Manufacturing & Research Spain, S.L.Registrant: Zoetis Inc	Carretera de Camprodon (L'hostal nou de Bianya), La Vall De, Bianya, Gerona 17813, Spain (ESP)	Analytical testing, Labelling, Finished drug manufacture, Packaging, sterilize	3001748505460052343
ZOETIS BELGIUM S.ARegistrant: Zoetis Inc	The Copse, RATHDRUM, , Ireland (IRL)	Analytical testing, Active ingredient (API) manufacture, Finished drug manufacture, particle size reduction	3015422006986062452
Zoetis Belgium S.a.Registrant: Zoetis Inc	Sragh Technology Park, Tullamore, Co. Offaly , Ireland (IRL)	Analytical testing, Active ingredient (API) manufacture, Finished drug manufacture	3015596301986062582
Zoetis Manufacturing Italia SRLRegistrant: Zoetis Inc	Via Gorgone Franco S.N.C., CATANIA, 95121, Italy (ITA)	Analytical testing, Active ingredient (API) manufacture, Packaging	3010097713339697390
ZOETIS INC.Registrant: Zoetis Inc	200 S GEOSPACE DR, INDEPENDENCE, Missouri (MO) 64056-3338, United States (USA)	Labelling, Packaging, Relabelling, Repackaging	3007919064079767221
Zoetis LLCRegistrant: Zoetis Inc	2605 E. Kilgore Road, Kalamazoo, Michigan (MI) 49001, United States (USA)	Analytical testing, Labelling, Finished drug manufacture, Packaging, Relabelling, Repackaging	3010146372079995959
ZOETISRegistrant: Zoetis Inc	1 Se Pfizer Way, Lees Summit, Missouri (MO) 64081, United States (USA)	Labelling, Packaging, Relabelling, Repackaging	1922097071419364
Zoetis Services LLCRegistrant: Zoetis Inc	1100 NW Main St, Lees Summit, Missouri (MO) 64086, United States (USA)	Labelling, Packaging, Relabelling, Repackaging	3030978447119241673
Zoetis LLCRegistrant: Zoetis Inc	601 West Cornhusker Highway, Lincoln, Nebraska (NE) 68521-3577, United States (USA)	Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging	1910179039055157

Catalogue

Drug listings by form and route

29 active NDC listings: 24 drug for further processing, 5 bulk ingredient. By marketing category: DRUG FOR FURTHER PROCESSING 19, BULK INGREDIENT 5, EXPORT ONLY 5.

Dosage form	NDCs
tablet, chewable	15
powder	4
tablet	3
tablet, coated	3
solution	2
liquid	1
paste	1

Route	NDCs

Labeller name on the listing	NDCs
zoetis inc.	29

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Bedinvetmab	solution	54771-2782BULK INGREDIENT
-	Doramectin	powder	54771-0207BULK INGREDIENT
-	Doxycycline	paste	54771-5246EXPORT ONLY
-	Malic Acid, Benzoic Acid, Salicylic Acid	solution	54771-7600DRUG FOR FURTHER PROCESSING
-	Moxidectin	powder	54771-7016BULK INGREDIENT
-	Nutritional Supplement	tablet	54771-8446EXPORT ONLY
-	Nutritional Supplement	tablet	54771-8448EXPORT ONLY
-	Nutritional Supplement	tablet	54771-8451EXPORT ONLY
-	Oclacitinib maleate	tablet, coated	54771-0495DRUG FOR FURTHER PROCESSING
-	Oclacitinib maleate	tablet, coated	54771-0496DRUG FOR FURTHER PROCESSING
-	Oclacitinib maleate	tablet, coated	54771-0497DRUG FOR FURTHER PROCESSING
-	Oclacitinib maleate	tablet, chewable	54771-1207DRUG FOR FURTHER PROCESSING
-	Oclacitinib maleate	tablet, chewable	54771-1208DRUG FOR FURTHER PROCESSING
-	Oclacitinib maleate	tablet, chewable	54771-1209DRUG FOR FURTHER PROCESSING
-	Oclacitinib maleate	powder	54771-1344BULK INGREDIENT
-	sarolaner	tablet, chewable	54771-1371DRUG FOR FURTHER PROCESSING
-	sarolaner	tablet, chewable	54771-1372DRUG FOR FURTHER PROCESSING
-	sarolaner	tablet, chewable	54771-1373DRUG FOR FURTHER PROCESSING
-	sarolaner	tablet, chewable	54771-1374DRUG FOR FURTHER PROCESSING
-	sarolaner	tablet, chewable	54771-1375DRUG FOR FURTHER PROCESSING
-	sarolaner	tablet, chewable	54771-1376DRUG FOR FURTHER PROCESSING
-	sarolaner	powder	54771-2716BULK INGREDIENT
-	sarolaner, moxidectin, and pyrantel	tablet, chewable	54771-2667DRUG FOR FURTHER PROCESSING
-	sarolaner, moxidectin, and pyrantel	tablet, chewable	54771-2668DRUG FOR FURTHER PROCESSING
-	sarolaner, moxidectin, and pyrantel	tablet, chewable	54771-2669DRUG FOR FURTHER PROCESSING
-	sarolaner, moxidectin, and pyrantel	tablet, chewable	54771-2670DRUG FOR FURTHER PROCESSING
-	sarolaner, moxidectin, and pyrantel	tablet, chewable	54771-2671DRUG FOR FURTHER PROCESSING
-	sarolaner, moxidectin, and pyrantel	tablet, chewable	54771-2684DRUG FOR FURTHER PROCESSING
-	vitamins	liquid	54771-8443EXPORT ONLY

Neighbours

Registered in the same town

Excite Pharma Services, LLCLEES SUMMIT, MO; Lees Summit, MO · 2 sites
Pfizer IncKalamazoo, MI
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.Catania, ITA
Haleon US Holdings LLCLincoln, NE
Dipharma Francis SrlKalamazoo, MI

Compare

Comparable companies in United States

The Procter & Gamble Manufacturing Company11 sites · 849 NDC
Pfizer Inc11 sites · 27 NDC
Sotera Health LLC11 sites · 2 NDC
Eli Lilly and Company10 sites · 189 NDC
Siegfried USA, LLC12 sites · 54 NDC
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.10 sites · 30 NDC
Medical-technical Gases, Inc.10 sites · 7 NDC
SOFIE Co. dba SOFIE12 sites · 5 NDC
Alcami Carolinas Corporation10 sites · 1 NDC
AbbVie Inc.13 sites · 131 NDC

Enquiry

Common questions

Is Zoetis Inc FDA approved?: Zoetis Inc holds 11 FDA-registered establishments across 6 countries. 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 Zoetis Inc's drugs manufactured?: At registered sites in Australia, Belgium, Spain, Ireland, Italy, the United States. The FDA register lists Rutherford; Ottignies-Louvain-la-Neuve; Bianya; The Copse; Tullamore; CATANIA, and 4 more. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging, particle size reduction, relabelling, repackaging, sterilize.
What drugs does Zoetis Inc make?: 29 products are listed under Zoetis Inc in the openFDA NDC Directory, most often as tablet, chewable; powder; tablet. 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.