Register entryRepackager / relabeller

XENEX LABORATORIES INC

Data as of · How to read this entry

Registered sites
1
Active NDC listings
38
Labeller names
2
Live patents
0
Countries
1
Base
Canada
Authorisation

Registered operations

Labelling1Packaging1Relabelling1Repackaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
XENEX LABORATORIES INC102-2440 CANOE AVE, COQUITLAM, BC V3K6C2, Canada (CAN)Labelling, Packaging, Relabelling, Repackaging3007170694209581065
Catalogue

Drug listings by form and route

38

38 active NDC listings: 37 bulk ingredient, 1 human otc drug. By marketing category: BULK INGREDIENT 37, OTC MONOGRAPH DRUG 1.

Dosage formNDCs
powder37
cream1
RouteNDCs
topical1
Labeller name on the listingNDCs
xenex laboratories inc37
xenex laboratories inc.1
Catalogue

Marketed products

38
BrandGeneric nameForm / routeNDC
-AMITRIPTYLINE HYDROCHLORIDEpowder68981-015BULK INGREDIENT
-AMLODIPINE BESYLATEpowder68981-016BULK INGREDIENT
-BACLOFENpowder68981-007BULK INGREDIENT
-BUDESONIDEpowder68981-017BULK INGREDIENT
-CLINDAMYCIN HYDROCHLORIDEpowder68981-004BULK INGREDIENT
-CLINDAMYCIN PHOSPHATEpowder68981-026BULK INGREDIENT
-CLOBETASOL PROPIONATE MICRONIZEDpowder68981-027BULK INGREDIENT
-CLONIDINE HYDROCHLORIDEpowder68981-029BULK INGREDIENT
-CLOTRIMAZOLEpowder68981-045BULK INGREDIENT
-CYCLOBENZAPRINE HYDROCHLORIDEpowder68981-008BULK INGREDIENT
-DICLOFENAC SODIUMpowder68981-003BULK INGREDIENT
-DILTIAZEM HYDROCHLORIDEpowder68981-018BULK INGREDIENT
-ERYTHROMYCINpowder68981-019BULK INGREDIENT
-ESTRADIOLpowder68981-012BULK INGREDIENT
-ESTRADIOLpowder68981-013BULK INGREDIENT
-FINASTERIDEpowder68981-021BULK INGREDIENT
-FLUOXETINE HYDROCHLORIDEpowder68981-044BULK INGREDIENT
-GABAPENTINpowder68981-009BULK INGREDIENT
-HYDROCORTISONEpowder68981-002BULK INGREDIENT
-KETOCONAZOLEpowder68981-023BULK INGREDIENT
-KETOPROFENpowder68981-031BULK INGREDIENT
-LIDOCAINEpowder68981-014BULK INGREDIENT
-LIDOCAINE HCL MONOHYDRATEpowder68981-011BULK INGREDIENT
-LOPERAMIDE HYDROCHLORIDEpowder68981-022BULK INGREDIENT
-MECLIZINE HYDROCHLORIDEpowder68981-024BULK INGREDIENT
-METRONIDAZOLEpowder68981-034BULK INGREDIENT
-MICONAZOLE NITRATEpowder68981-035BULK INGREDIENT
-MINOXIDILpowder68981-036BULK INGREDIENT
-NALTREXONE HYDROCHLORIDEpowder68981-037BULK INGREDIENT
-NAPROXEN BASEpowder68981-038BULK INGREDIENT
-NIFEDIPINEpowder68981-039BULK INGREDIENT
-OMEPRAZOLEpowder68981-006BULK INGREDIENT
-PHENAZOPYRIDINE HCLpowder68981-046BULK INGREDIENT
-PIROXICAMpowder68981-041BULK INGREDIENT
-PROGESTERONEpowder68981-005BULK INGREDIENT
-SILDENAFIL CITRATEpowder68981-001BULK INGREDIENT
-TADALAFILpowder68981-043BULK INGREDIENT
XENCARE INFLAMAX NATURAL TOPICAL PAINMENTHOL, CAPSAICINcream, topical68981-900OTC MONOGRAPH DRUG
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Enquiry

Common questions

Is XENEX LABORATORIES INC FDA approved?
XENEX LABORATORIES INC holds 1 FDA-registered establishment in Canada. 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 XENEX LABORATORIES INC's registered sites?
The FDA register lists COQUITLAM. Registered operations: labelling, packaging, relabelling, repackaging.
What drugs does XENEX LABORATORIES INC make?
38 products are listed under XENEX LABORATORIES INC in the openFDA NDC Directory, most often as powder; cream. 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.