Register entry

Dee Cee Laboratories, Inc

Data as of · How to read this entry

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

Registered operations

Labelling1Finished drug manufacture1Packaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Dee Cee Laboratories, Inc.Registrant: Dee Cee Laboratories, Inc304 Dee Cee Court, White House, Tennessee (TN) 37188, United States (USA)Labelling, Finished drug manufacture, Packaging1023013034731893
Catalogue

Marketed products

1
BrandGeneric nameForm / routeNDC
Formula 303Valerian Root, Passiflora, Magnesium Carbonatetablet, oral52301-303UNAPPROVED HOMEOPATHIC
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Enquiry

Common questions

Is Dee Cee Laboratories, Inc FDA approved?
Dee Cee Laboratories, 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 Dee Cee Laboratories, Inc's drugs manufactured?
The FDA register lists White House, TN. Registered operations: labelling, finished drug manufacture, packaging.
What drugs does Dee Cee Laboratories, Inc make?
1 product is listed under Dee Cee Laboratories, Inc in the openFDA NDC Directory, most often as 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.