Register entry

Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals)

Data as of · How to read this entry

Registered sites
0
Active NDC listings
10
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

10

10 active NDC listings: 10 human prescription drug. By marketing category: NDA 8, ANDA 2.

Dosage formNDCs
tablet4
granule, for suspension2
suspension2
tablet, extended release2
RouteNDCs
oral10
Labeller name on the listingNDCs
azurity pharmaceuticals, inc. (formerly arbor pharmaceuticals)10
Catalogue

Marketed products

10
BrandGeneric nameForm / routeNDC
E.E.SErythromycin Ethylsuccinategranule, for suspension, oral24338-134NDA
E.E.SErythromycin Ethylsuccinategranule, for suspension, oral24338-136NDA
E.E.S 400Erythromycin Ethylsuccinatetablet, oral24338-100ANDA
ERYTHROMYCIN ETHYLSUCCINATEErythromycin Ethylsuccinatetablet, oral24338-110ANDA
EdarbyclorAzilsartan kamedoxomil and chlorthalidonetablet, oral60631-412NDA
EdarbyclorAzilsartan kamedoxomil and chlorthalidonetablet, oral60631-425NDA
Ery-PedErythromycin Ethylsuccinatesuspension, oral24338-130NDA
Ery-PedErythromycin Ethylsuccinatesuspension, oral24338-132NDA
Horizantgabapentin enacarbiltablet, extended release, oral53451-0101NDA
Horizantgabapentin enacarbiltablet, extended release, oral53451-0103NDA
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Other companies listing erythromycin ethylsuccinate

Enquiry

Common questions

Is Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) FDA approved?
Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) holds no registered establishment of its own; 10 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) make?
10 products are listed under Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals) in the openFDA NDC Directory, most often as tablet; granule, for suspension; suspension. 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.