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DEXTROMETHORPHAN HYDROBROMIDE au Canada

739 fiches de médicaments provenant de 96 titulaires portent ce nom dans les sources officielles. Collectées le 11 novembre 2026.

Médicaments, page 8

Titulaires et statut de ces fiches
Nom Titulaire Statut Code
DM PLUS DECONGESTANT COUGH SYRUP · 30 MG per 5 ML + 15 MG per 5 ML · SYRUP TECHNILAB PHARMA INC. cancelled DIN 02072823Code de médicament DPD 17792
DM PLUS DECONGESTANT PLUS EXPECTORANT COUGH SYRUP · 100 MG per 5 ML + 30 MG per 5 ML + 15 MG per 5 ML · SYRUP TECHNILAB PHARMA INC. cancelled DIN 02097338Code de médicament DPD 17791
DM PLUS DECONGESTANT PLUS EXPECTOR.EX.ST.SYR · 200 MG per 5 ML + 30 MG per 5 ML + 15 MG per 5 ML · SYRUP TECHNILAB PHARMA INC. cancelled DIN 02136619Code de médicament DPD 17790
DM PLUS EXPECTORANT SYRUP · 100 MG per 5 ML + 15 MG per 5 ML · SYRUP TECHNILAB PHARMA INC. cancelled DIN 02136430Code de médicament DPD 17793
DM SANS SUCRE LIQ 15MG/5ML · 15 MG per 5 ML · LIQUID LABORATOIRES TRIANON INC. authorised DIN 00511013Code de médicament DPD 9543
DM SYRUP · 15 MG per 5 ML + 125 MG per 5 ML + 12.5 MG per 5 ML · SYRUP TECHNILAB PHARMA INC. cancelled DIN 00687677Code de médicament DPD 7126
DM SYRUP · 15 MG per 5 ML · SYRUP TEVA CANADA LIMITED cancelled DIN 00800813Code de médicament DPD 10054
DM SYRUP (SUCROSE FREE) · 15 MG per 5 ML · SYRUP TEVA CANADA LIMITED cancelled DIN 01952137Code de médicament DPD 12621
DR. COCOA FOR CHILDREN DAYTIME COUGH + COLD · 2.5 MG per 5 ML + 5.0 MG per 5 ML · SYRUP INFIRST HEALTHCARE INC cancelled DIN 02436574Code de médicament DPD 92090
DR. COCOA FOR CHILDREN LONG-ACTING COUGH · 7.5 MG per 5 ML · SYRUP INFIRST HEALTHCARE INC cancelled DIN 02436582Code de médicament DPD 92091
DRISTAN DM · 15 MG · TABLET WYETH CONSUMER HEALTHCARE INC. cancelled DIN 02272148Code de médicament DPD 75767
DRIXORAL COUGH LIQUID CAPS - 30MG · 30 MG · CAPSULE SCHERING-PLOUGH CANADA INC cancelled DIN 02146614Code de médicament DPD 19412
DRY COUGH · 7.5 MG per 5 ML · SOLUTION ACCUDIAL PHARMACEUTICAL INC cancelled DIN 02378647Code de médicament DPD 86444
DRY COUGH CAPSULES · 15 MG · CAPSULE CELLCHEM PHARMACEUTICALS INC. authorised DIN 02542889Code de médicament DPD 103140
DRY COUGH & COLD SYRUP · 15 MG per 5 ML + 30 MG per 5 ML · SYRUP CELLCHEM PHARMACEUTICALS INC. authorised DIN 02258668Code de médicament DPD 74385
DRY COUGH RELIEF EXTRA STRENGTH · 30 MG per 10 ML · SYRUP CRLS authorised DIN 02534754Code de médicament DPD 102364
DRY COUGH RELIEF EXTRA STRENGTH · 30 MG per 10 ML · SYRUP TRILLIUM HEALTH CARE PRODUCTS INC authorised DIN 02405946Code de médicament DPD 89069
DRY COUGH SYRUP · 15 MG per 5 ML · SYRUP CELLCHEM PHARMACEUTICALS INC. authorised DIN 02261294Code de médicament DPD 74668
EQUATE DAYTIME LIQUID CAPSULES · 30 MG + 15 MG + 325 MG · CAPSULE IVAX PHARMACEUTICALS INCORPORATED cancelled DIN 02272350Code de médicament DPD 75787
EQUATE NIGHTTIME LIQUID CAPSULES · 6.25 MG + 30 MG + 325 MG + 15 MG · CAPSULE IVAX PHARMACEUTICALS INCORPORATED cancelled DIN 02272369Code de médicament DPD 75788
EXPECTORANT DM COUGH EXTRA STRENGTH · 15 MG per 5 ML + 200 MG per 5 ML · SYRUP TANTA PHARMACEUTICALS INC authorised DIN 02370824Code de médicament DPD 85594
EXPECTORANT DM COUGH EXTRA STRENGTH WITH DECONGESTANT · 15 MG per 5 ML + 30 MG per 5 ML + 200 MG per 5 ML · SYRUP TANTA PHARMACEUTICALS INC authorised DIN 02371014Code de médicament DPD 85620
EXPECTORANT DM COUGH SYRUP · 100 MG per 5 ML + 15 MG per 5 ML · SYRUP TANTA PHARMACEUTICALS INC authorised DIN 00833258Code de médicament DPD 14485
EXTRA STRENGTH COLD MEDICATION DAY TIME RELIEF · 10 MG + 5 MG + 500 MG · TABLET GENVION CORPORATION authorised DIN 02426188Code de médicament DPD 91078
EXTRA STRENGTH COLD MEDICATION DAYTIME RELIEF · 15 MG + 30 MG + 500 MG · TABLET VITA HEALTH PRODUCTS INC authorised DIN 02083736Code de médicament DPD 17880
EXTRA STRENGTH COLD MEDICATION DAYTIME RLF · 30 MG + 15 MG + 500 MG · TABLET STANLEY PHARMACEUTICALS, A DIVISION OF VITA HEALTH PRODUCTS INC. cancelled DIN 02171325Code de médicament DPD 19562
EXTRA STRENGTH COLD MEDICATION NIGHT TIME RELIEF · 500 MG + 10 MG + 2 MG + 5 MG · TABLET GENVION CORPORATION authorised DIN 02426250Code de médicament DPD 91085
EXTRA STRENGTH COLD MEDICATION NIGHTTIME RELIEF · 500 MG + 2 MG + 30 MG + 15 MG · TABLET VITA HEALTH PRODUCTS INC authorised DIN 02039842Code de médicament DPD 17887
EXTRA STRENGTH COLD MEDICATION NIGHTTIME RLF · 15 MG + 500 MG + 30 MG + 2 MG · TABLET STANLEY PHARMACEUTICALS, A DIVISION OF VITA HEALTH PRODUCTS INC. cancelled DIN 02171317Code de médicament DPD 19561
EXTRA STRENGTH CONTAC COMPLETE COUGH, COLD & FLU · 500 MG + 5 MG + 15 MG · TABLET VALEANT CANADA LP / VALEANT CANADA S.E.C. cancelled DIN 02276224Code de médicament DPD 76189
EXTRA STRENGTH COUGH PLUS COLD RELIEF SYRUP · 15 MG per 5 ML + 200 MG per 5 ML + 30 MG per 5 ML · SYRUP CELLCHEM PHARMACEUTICALS INC. authorised DIN 02263122Code de médicament DPD 74853
EXTRA STRENGTH DAY AND NIGHT COLD MEDICATION · 30 MG + 2 MG + 15 MG + 500 MG · KIT / TABLET PENDOPHARM DIVISION OF PHARMASCIENCE INC cancelled DIN 02309610Code de médicament DPD 79527
EXTRA STRENGTH DAYTIME COLD RELIEF · 30 MG + 15 MG + 500 MG · TABLET PENDOPHARM DIVISION OF PHARMASCIENCE INC cancelled DIN 02243221Code de médicament DPD 67104
EXTRA STRENGTH DAYTIME COLD RELIEF-CAPLET · 30 MG + 500 MG + 15 MG · TABLET KSL PHARMACEUTICALS cancelled DIN 02172364Code de médicament DPD 19107
EXTRA STRENGTH DAYTIME COLD RELIEF PE · 500 MG + 5 MG + 10 MG · TABLET VITA HEALTH PRODUCTS INC cancelled DIN 02293099Code de médicament DPD 77847
EXTRA STRENGTH DAYTIME FLU PE · 5 MG + 500 MG + 10 MG · TABLET VITA HEALTH PRODUCTS INC cancelled DIN 02293552Code de médicament DPD 77891
EXTRA STRENGTH DM COUGH AND COLD LIQUID · 10.0 MG per 5 ML + 4.0 MG per 5 ML + 20.0 MG per 5 ML · SOLUTION TANTA PHARMACEUTICALS INC authorised DIN 02267454Code de médicament DPD 75286
EXTRA STRENGTH DM COUGH AND COLD SYRUP · 10 MG per 5 ML + 20 MG per 5 ML + 4 MG per 5 ML · SYRUP JAMP PHARMA CORPORATION authorised DIN 02266474Code de médicament DPD 75190
EXTRA STRENGTH FLU RELIEF DAYTIME · 500 MG + 30 MG + 15 MG · TABLET VITA HEALTH PRODUCTS INC authorised DIN 02248580Code de médicament DPD 72935
EXTRA STRENGTH MUCOUS RELIEF COUGH · 400 MG + 20 MG · TABLET TEVA CANADA LIMITED cancelled DIN 02353563Code de médicament DPD 83878
EXTRA STRENGTH NEOCITRAN FLU NIGHT · 60 MG per PCK + 20 MG per PCK + 650 MG per PCK + 4 MG per PCK · PACKAGE / POWDER NOVARTIS CONSUMER HEALTH CANADA INC. cancelled DIN 02196174Code de médicament DPD 35886
EXTRA STRENGTH NEOCITRAN TOTAL NIGHT · 4 MG per PCK + 20 MG per PCK + 60 MG per PCK + 650 MG per PCK · POWDER FOR SOLUTION NOVARTIS CONSUMER HEALTH CANADA INC. cancelled DIN 02266024Code de médicament DPD 75146
EXTRA STRENGTH NEOCITRAN TOTAL SYRUP · 20 MG per 30 ML + 10 MG per 30 ML + 650 MG per 30 ML · SYRUP NOVARTIS CONSUMER HEALTH CANADA INC. cancelled DIN 02275988Code de médicament DPD 76166
EXTRA STRENGTH NIGHTTIME COLD RELIEF · 15 MG + 30 MG + 500 MG + 2 MG · TABLET PENDOPHARM DIVISION OF PHARMASCIENCE INC cancelled DIN 02244142Code de médicament DPD 68103
EXTRA STRENGTH NIGHTTIME COLD RELIEF-CAPLET · 30 MG + 500 MG + 2 MG + 15 MG · TABLET KSL PHARMACEUTICALS cancelled DIN 02171406Code de médicament DPD 19104
EXTRA STRENGTH NIGHTTIME COLD RELIEF PE · 2 MG + 5 MG + 500 MG + 10 MG · TABLET VITA HEALTH PRODUCTS INC cancelled DIN 02293110Code de médicament DPD 77849
EXTRA STRENGTH NIGHTTIME FLU PE · 10 MG + 500 MG + 5 MG + 2 MG · TABLET VITA HEALTH PRODUCTS INC cancelled DIN 02293560Code de médicament DPD 77892
EXTRA STRENGTH TYLENOL COLD AND FLU DAYTIME · 10 MG per 30 ML + 1000 MG per 30 ML + 20 MG per 30 ML · LIQUID MCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC cancelled DIN 02276666Code de médicament DPD 76234
EXTRA STRENGTH TYLENOL COLD AND FLU NIGHTTIME · 1000 MG per 30 ML + 12.5 MG per 30 ML + 10 MG per 30 ML + 20 MG per 30 ML · LIQUID MCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC cancelled DIN 02276887Code de médicament DPD 76255
EXTRA STRENGTH TYLENOL COLD AND FLU POWDER · 1 G per PCK + 4 MG per PCK + 30 MG per PCK + 60 MG per PCK · POWDER FOR SOLUTION MCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC cancelled DIN 01938169Code de médicament DPD 13002

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