Register entryRepackager / relabeller

CLINICAL SOLUTIONS WHOLESALE, LLC

Data as of · How to read this entry

Registered sites
1
Active NDC listings
67
Live patents
0
Countries
1
Base
United States
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
CLINICAL SOLUTIONS WHOLESALE, LLC416 Mary Lindsay Polk Dr Ste 519, Franklin, Tennessee (TN) 37067, United States (USA)Repackaging3010191394078710347
Catalogue

Drug listings by form and route

67

67 active NDC listings: 67 human prescription drug. By marketing category: ANDA 61, UNAPPROVED DRUG OTHER 6.

Dosage formNDCs
tablet42
capsule20
tablet, film coated4
tablet, coated1
RouteNDCs
oral56
sublingual11
Labeller name on the listingNDCs
clinical solutions wholesale, llc67
Catalogue

Marketed products

67
BrandGeneric nameForm / routeNDC
ACETAMINOPHEN AND CODEINE PHOSPHATEacetaminophen and codeine phosphatetablet, oral58118-0485ANDA
ACETAMINOPHEN AND CODEINE PHOSPHATEacetaminophen and codeine phosphatetablet, oral58118-4484ANDA
AlprazolamAlprazolamtablet, oral58118-0676ANDA
AlprazolamAlprazolamtablet, oral58118-0677ANDA
AlprazolamAlprazolamtablet, oral58118-0678ANDA
AlprazolamAlprazolamtablet, oral58118-0679ANDA
BUPRENORPHINEBUPRENORPHINEtablet, sublingual58118-0501ANDA
BUPRENORPHINEBUPRENORPHINEtablet, sublingual58118-0502ANDA
BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATEBUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATEtablet, sublingual58118-0549ANDA
BuprenorphineBuprenorphinetablet, sublingual58118-0460ANDA
BuprenorphineBuprenorphinetablet, sublingual58118-4459ANDA
Buprenorphine HClBuprenorphine HCltablet, sublingual58118-0176ANDA
Buprenorphine HClBuprenorphine HCltablet, sublingual58118-0177ANDA
Buprenorphine Hydrochloride and Naloxone Hydrochloride DihydrateBuprenorphine Hydrochloride and Naloxone Hydrochloride Dihydratetablet, sublingual58118-8005ANDA
Buprenorphine Hydrochloride and Naloxone Hydrochloride DihydrateBuprenorphine Hydrochloride and Naloxone Hydrochloride Dihydratetablet, sublingual58118-8020ANDA
Chlordiazepoxide HydrochlorideChlordiazepoxide Hydrochloridecapsule, oral58118-1033ANDA
Chlordiazepoxide HydrochlorideChlordiazepoxide Hydrochloridecapsule, oral58118-1590ANDA
ClonazepamClonazepamtablet, oral58118-0152ANDA
ClonazepamClonazepamtablet, oral58118-0153ANDA
ClonazepamClonazepamtablet, oral58118-0154ANDA
ClonazepamClonazepamtablet, oral58118-0832ANDA
Clorazepate DipotassiumClorazepate Dipotassiumtablet, oral58118-4042ANDA
Clorazepate DipotassiumClorazepate Dipotassiumtablet, oral58118-4043ANDA
Clorazepate DipotassiumClorazepate Dipotassiumtablet, oral58118-4044ANDA
DiazepamDiazepamtablet, oral58118-3925ANDA
DiazepamDiazepamtablet, oral58118-3926ANDA
Diazepamdiazepamtablet, oral58118-4047ANDA
GABAPENTINGabapentintablet, oral58118-0166ANDA
GABAPENTINGabapentintablet, oral58118-1167ANDA
GabapentinGabapentincapsule, oral58118-1102ANDA
GabapentinGabapentincapsule, oral58118-1103ANDA
GabapentinGabapentincapsule, oral58118-2101ANDA
GabapentinGabapentintablet, oral58118-2126ANDA
GabapentinGabapentintablet, oral58118-2127ANDA
GabapentinGabapentincapsule, oral58118-3224ANDA
LACOSAMIDELACOSAMIDEtablet, film coated, oral58118-8812ANDA
LACOSAMIDELACOSAMIDEtablet, film coated, oral58118-8813ANDA
LACOSAMIDELACOSAMIDEtablet, film coated, oral58118-8814ANDA
LACOSAMIDELACOSAMIDEtablet, film coated, oral58118-8815ANDA
LorazepamLorazepamtablet, oral58118-0773ANDA
LorazepamLorazepamtablet, oral58118-0774ANDA
LorazepamLorazepamtablet, oral58118-0904ANDA
LorazepamLorazepamtablet, oral58118-1095ANDA
LorazepamLorazepamtablet, oral58118-1096ANDA
PHENOBARBITALPHENOBARBITALtablet, oral58118-0572UNAPPROVED DRUG OTHER
PHENOBARBITALPHENOBARBITALtablet, oral58118-0573UNAPPROVED DRUG OTHER
PHENOBARBITALPHENOBARBITALtablet, oral58118-0574UNAPPROVED DRUG OTHER
PHENOBARBITALPHENOBARBITALtablet, oral58118-0576UNAPPROVED DRUG OTHER
Phenobarbitalphenobarbitaltablet, oral58118-0626UNAPPROVED DRUG OTHER
Phenobarbitalphenobarbitaltablet, oral58118-1626UNAPPROVED DRUG OTHER
PregabalinPregabalincapsule, oral58118-0758ANDA
PregabalinPregabalincapsule, oral58118-0759ANDA
PregabalinPregabalincapsule, oral58118-0760ANDA
PregabalinPregabalincapsule, oral58118-0761ANDA
PregabalinPregabalincapsule, oral58118-0762ANDA
PregabalinPregabalincapsule, oral58118-0763ANDA
PregabalinPregabalincapsule, oral58118-0764ANDA
PregabalinPregabalincapsule, oral58118-0765ANDA
PregabalinPregabalincapsule, oral58118-1462ANDA
PregabalinPregabalincapsule, oral58118-1463ANDA
PregabalinPregabalincapsule, oral58118-1464ANDA
PregabalinPregabalincapsule, oral58118-1465ANDA
PregabalinPregabalincapsule, oral58118-1466ANDA
PregabalinPregabalincapsule, oral58118-1467ANDA
Tramadol HydrochlorideTramadol Hydrochloridetablet, coated, oral58118-2348ANDA
buprenorphine hydrochloride and naloxone hydrochloride dihydratebuprenorphine hydrochloride and naloxone hydrochloride dihydratetablet, sublingual58118-1188ANDA
buprenorphine hydrochloride and naloxone hydrochloride dihydratebuprenorphine hydrochloride and naloxone hydrochloride dihydratetablet, sublingual58118-1189ANDA
Neighbours

Registered in the same town

1
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Enquiry

Common questions

Is CLINICAL SOLUTIONS WHOLESALE, LLC FDA approved?
CLINICAL SOLUTIONS WHOLESALE, 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 CLINICAL SOLUTIONS WHOLESALE, LLC's registered sites?
The FDA register lists Franklin, TN. Registered operations: repackaging.
What drugs does CLINICAL SOLUTIONS WHOLESALE, LLC make?
67 products are listed under CLINICAL SOLUTIONS WHOLESALE, LLC in the openFDA NDC Directory, most often as tablet; capsule; tablet, film 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.