Is KITE PHARMA, INC. FDA approved?

KITE PHARMA, INC. holds 5 FDA-registered establishments across 2 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 KITE PHARMA, INC.'s drugs manufactured?

At registered sites in the Netherlands, the United States. The FDA register lists Hoofddorp; EL SEGUNDO, CA; Frederick, MD; Oceanside, CA; Santa Monica, CA. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.

What drugs does KITE PHARMA, INC. make?

3 products are listed under KITE PHARMA, INC. in the openFDA NDC Directory, most often as suspension. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

KITE PHARMA, INC.

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

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Registered sites: 5
Active NDC listings: 3
Live patents: 0
Countries: 2
Base: United States

Authorisation

Registered operations

Analytical testing5Active ingredient (API) manufacture1Labelling3Finished drug manufacture2Packaging3

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Kite Pharma EU B.V.Registrant: KITE PHARMA, INC.	Tufsteen 1, Hoofddorp, NT 2132, Netherlands (NLD)	Analytical testing, Labelling, Packaging	3018906348491405777
KITE PHARMA, INC.	2355 UTAH AVE, EL SEGUNDO, California (CA) 90245, United States (USA)	Analytical testing, Labelling, Finished drug manufacture, Packaging	3012583739080315797
Kite Pharma, Inc.Registrant: KITE PHARMA, INC.	9021 Bennett Creek Blvd, Frederick, Maryland (MD) 21704, United States (USA)	Analytical testing, Labelling, Finished drug manufacture, Packaging	3016888173117989834
Gilead Sciences, Inc.Registrant: KITE PHARMA, INC.	4010 Ocean Ranch Blvd, Oceanside, California (CA) 92056, United States (USA)	Analytical testing, Active ingredient (API) manufacture	3012871330117649816
Kite Pharma, Inc.Registrant: KITE PHARMA, INC.	1800 Stewart St., Santa Monica, California (CA) 90404, United States (USA)	Analytical testing	3014007584116931311

Catalogue

Drug listings by form and route

3 active NDC listings: 3 cellular therapy. By marketing category: BLA 3.

Dosage form	NDCs
suspension	3

Route	NDCs
intravenous	3

Labeller name on the listing	NDCs
kite pharma, inc.	3

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
TECARTUS	brexucabtagene autoleucel	suspension, intravenous	71287-219BLA
TECARTUS	brexucabtagene autoleucel	suspension, intravenous	71287-220BLA
YESCARTA	axicabtagene ciloleucel	suspension, intravenous	71287-119BLA

Neighbours

Registered in the same town

AstraZeneca PLCFrederick, MD
Arcet Equipment Company dba Arc3 Gases NorthFrederick, MD
Genentech, Inc.Oceanside, CA
COSMETIX WESTEl Segundo, CA
Precision Stability Storage, LLCEl Segundo, CA
Modavar Pharmaceuticals LLCFrederick, MD

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Enquiry

Common questions

Is KITE PHARMA, INC. FDA approved?: KITE PHARMA, INC. holds 5 FDA-registered establishments across 2 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 KITE PHARMA, INC.'s drugs manufactured?: At registered sites in the Netherlands, the United States. The FDA register lists Hoofddorp; EL SEGUNDO, CA; Frederick, MD; Oceanside, CA; Santa Monica, CA. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.
What drugs does KITE PHARMA, INC. make?: 3 products are listed under KITE PHARMA, INC. in the openFDA NDC Directory, most often as suspension. 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.