Register entryRepackager / relabeller

Boxout, LLC

Data as of · How to read this entry

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

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Boxout, LLC6333 Hudson Crossing Parkway, Hudson, Ohio (OH) 44236, United States (USA)Packaging3008492870066689993
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
BodyMed Alcohol Prep PadAlcohol Prep Padswab, topical82308-001OTC MONOGRAPH DRUG
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Common questions

Is Boxout, LLC FDA approved?
Boxout, LLC 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 Boxout, LLC's registered sites?
The FDA register lists Hudson, OH. Registered operations: packaging.
What drugs does Boxout, LLC make?
1 product is listed under Boxout, LLC in the openFDA NDC Directory, most often as swab. 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.