Register entry

Braeburn Inc.

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Registered sites
0
Active NDC listings
7
Live patents
49
Countries
0
Catalogue

Drug listings by form and route

7

7 active NDC listings: 7 human prescription drug. By marketing category: NDA 7.

Dosage formNDCs
injection7
RouteNDCs
subcutaneous7
Labeller name on the listingNDCs
braeburn inc.7
Exclusivity

Patents and exclusivities

49
PatentProductCoversExpiry
8236292BRIXADIbuprenorphineproductJan 2027
10912772BRIXADIbuprenorphineuseJul 2032
11110084BRIXADIbuprenorphineproductJul 2032
11135215BRIXADIbuprenorphineproductJul 2032
12161640BRIXADIbuprenorphineproductJul 2032
12318379BRIXADIbuprenorphineproductJul 2032
9937164BRIXADIbuprenorphineproductJul 2032
Catalogue

Marketed products

7
BrandGeneric nameForm / routeNDC
BRIXADIBUPRENORPHINEinjection, subcutaneous58284-208NDA
BRIXADIBUPRENORPHINEinjection, subcutaneous58284-216NDA
BRIXADIBUPRENORPHINEinjection, subcutaneous58284-224NDA
BRIXADIBUPRENORPHINEinjection, subcutaneous58284-228NDA
BRIXADIBUPRENORPHINEinjection, subcutaneous58284-232NDA
BRIXADIBUPRENORPHINEinjection, subcutaneous58284-264NDA
BRIXADIBUPRENORPHINEinjection, subcutaneous58284-296NDA
Compare

Other companies listing buprenorphine

Enquiry

Common questions

Is Braeburn Inc. FDA approved?
Braeburn Inc. holds no registered establishment of its own; 7 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Braeburn Inc. make?
7 products are listed under Braeburn Inc. in the openFDA NDC Directory, most often as injection. 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.