Register entryRepackager / relabeller

DOC Brands

Data as of · How to read this entry

Registered sites
1
Active NDC listings
2
Live patents
0
Countries
1
Base
United States
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
DOC Brands10334 Cogdill Rd, Knoxville, Tennessee (TN) 37932-3305, United States (USA)Relabelling3015128224081254601
Catalogue

Drug listings by form and route

2

2 active NDC listings: 2 human otc drug. By marketing category: OTC MONOGRAPH DRUG 2.

Dosage formNDCs
tablet, extended release2
RouteNDCs
oral2
topical2
Labeller name on the listingNDCs
doc brands2
Catalogue

Marketed products

2
BrandGeneric nameForm / routeNDC
Dentemp Canker CoverCanker Covertablet, extended release, oral, topical73653-210OTC MONOGRAPH DRUG
Dentemp Canker CoverCanker Covertablet, extended release, oral, topical73653-213OTC MONOGRAPH DRUG
Neighbours

Registered in the same town

7
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Comparable companies in United States

Enquiry

Common questions

Is DOC Brands FDA approved?
DOC Brands 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 DOC Brands's registered sites?
The FDA register lists Knoxville, TN. Registered operations: relabelling.
What drugs does DOC Brands make?
2 products are listed under DOC Brands in the openFDA NDC Directory, most often as tablet, extended release. 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.