Register entry

Oxford Pharmaceuticals, LLC

Data as of · How to read this entry

Registered sites
1
Active NDC listings
35
Live patents
0
Countries
1
Base
United States
Authorisation

Registered operations

Analytical testing1Labelling1Finished drug manufacture1Packaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Oxford Pharmaceuticals, LLC301 Leaf Lake Parkway, Birmingham, Alabama (AL) 35211, United States (USA)Analytical testing, Labelling, Finished drug manufacture, Packaging3012257735079638266
Catalogue

Drug listings by form and route

35

35 active NDC listings: 35 human prescription drug. By marketing category: ANDA 35.

Dosage formNDCs
tablet23
tablet, film coated9
tablet, coated3
RouteNDCs
oral35
Labeller name on the listingNDCs
oxford pharmaceuticals, llc35
Catalogue

Marketed products

35
BrandGeneric nameForm / routeNDC
AMLODIPINE BESYLATE 10 mgAMLODIPINE BESYLATEtablet, oral69584-023ANDA
AMLODIPINE BESYLATE 2.5 mgAMLODIPINE BESYLATEtablet, oral69584-021ANDA
AMLODIPINE BESYLATE 5 mgAMLODIPINE BESYLATEtablet, oral69584-022ANDA
Buspirone Hydrochloridebuspirone hydrochloridetablet, oral69584-091ANDA
Buspirone Hydrochloridebuspirone hydrochloridetablet, oral69584-092ANDA
Buspirone Hydrochloridebuspirone hydrochloridetablet, oral69584-093ANDA
Buspirone Hydrochloridebuspirone hydrochloridetablet, oral69584-094ANDA
CarisoprodolCarisoprodoltablet, oral69584-111ANDA
DipyridamoleDipyridamoletablet, film coated, oral69584-181ANDA
DipyridamoleDipyridamoletablet, film coated, oral69584-182ANDA
DipyridamoleDipyridamoletablet, film coated, oral69584-183ANDA
GlipizideGlipizidetablet, oral69584-309ANDA
GlipizideGlipizidetablet, oral69584-310ANDA
HydrochlorothiazideHydrochlorothiazidetablet, oral69584-361ANDA
HydrochlorothiazideHydrochlorothiazidetablet, oral69584-362ANDA
Imipramine HydrochlorideImipramine Hydrochloridetablet, oral69584-425ANDA
Imipramine HydrochlorideImipramine Hydrochloridetablet, oral69584-426ANDA
Imipramine HydrochlorideImipramine Hydrochloridetablet, oral69584-427ANDA
Methocarbamolmethocarbamoltablet, oral69584-611ANDA
Methocarbamolmethocarbamoltablet, oral69584-612ANDA
PrimidonePrimidonetablet, oral69584-684ANDA
PrimidonePrimidonetablet, oral69584-685ANDA
Sotalol HydrochlorideSotalol Hydrochloridetablet, oral69584-841ANDA
Sotalol HydrochlorideSotalol Hydrochloridetablet, oral69584-842ANDA
Sotalol HydrochlorideSotalol Hydrochloridetablet, oral69584-843ANDA
Sotalol HydrochlorideSotalol Hydrochloridetablet, oral69584-844ANDA
SpironolactoneSpironolactonetablet, coated, oral69584-852ANDA
SpironolactoneSpironolactonetablet, coated, oral69584-853ANDA
SpironolactoneSpironolactonetablet, coated, oral69584-854ANDA
Trazodone HydrochlorideTrazodone Hydrochloridetablet, film coated, oral69584-884ANDA
Trazodone HydrochlorideTrazodone Hydrochloridetablet, film coated, oral69584-885ANDA
paroxetine hydrochlorideparoxetine hydrochloridetablet, film coated, oral69584-671ANDA
paroxetine hydrochlorideparoxetine hydrochloridetablet, film coated, oral69584-672ANDA
paroxetine hydrochlorideparoxetine hydrochloridetablet, film coated, oral69584-673ANDA
paroxetine hydrochlorideparoxetine hydrochloridetablet, film coated, oral69584-674ANDA
Neighbours

Registered in the same town

6
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Comparable companies in United States

Enquiry

Common questions

Is Oxford Pharmaceuticals, LLC FDA approved?
Oxford Pharmaceuticals, 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 Oxford Pharmaceuticals, LLC's drugs manufactured?
The FDA register lists Birmingham, AL. Registered operations: analytical testing, labelling, finished drug manufacture, packaging.
What drugs does Oxford Pharmaceuticals, LLC make?
35 products are listed under Oxford Pharmaceuticals, LLC in the openFDA NDC Directory, most often as tablet; tablet, film coated; tablet, coated. 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.