Is CellTrans Inc. FDA approved?

CellTrans 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 CellTrans Inc.'s drugs manufactured?

The FDA register lists Chicago, IL. Registered operations: active ingredient (API) manufacture.

What drugs does CellTrans Inc. make?

1 product is listed under CellTrans Inc. in the openFDA NDC Directory, most often as solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

CellTrans Inc.

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

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Registered sites: 1
Active NDC listings: 1
Live patents: 0
Countries: 1
Base: United States

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
CellTrans Inc.	1740 W. Taylor St, Ste C200, Chicago, Illinois (IL) 60612, United States (USA)	Active ingredient (API) manufacture	3019202665117774787

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
LANTIDRA	DONISLECEL	solution, intravascular	73539-001BLA

Neighbours

Registered in the same town

Ecolab Inc.Chicago, IL
Bajaj Healthcare LtdChicago, IL
Kashiv BioSciences, LLCChicago, IL
AltaThera Pharmaceuticals LLCChicago, IL
Korex Chicago LLCChicago, IL
Primrose Candy CompanyChicago, IL

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Enquiry

Common questions

Is CellTrans Inc. FDA approved?: CellTrans 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 CellTrans Inc.'s drugs manufactured?: The FDA register lists Chicago, IL. Registered operations: active ingredient (API) manufacture.
What drugs does CellTrans Inc. make?: 1 product is listed under CellTrans Inc. in the openFDA NDC Directory, most often as 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.