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Search: National Drug Schedules

Begin your search by using the generic name of the product:

Search by Glossary
Drug Name Comment Schedule Date
Econazole or its salts I DEC / 13
Ecothiophate or its salts I DEC / 13
Ectylurea or its salts I DEC / 13
Eculizumab I DEC / 13
Edaravone or its derivatives I NOV / 19
Edoxaban or its salts I FEB / 17
Edrophonium chloride I DEC / 13
Efalizumab I DEC / 13
Efavirenz I DEC / 13
Efinaconazole I DEC / 13
Eflornithine or its salts or derivatives I DEC / 13
Elagolix or its salts I DEC / 18
Elbasvir or its salts I AUG / 16
Eletriptan or its salts I DEC / 13
Eliglustat or its salts I MAY / 17
Elosulfase alfa I AUG / 14
Elotuzumab I AUG / 16
Eltrombopag or its salts

including but not limited to eltrombopag olamine

I DEC / 13
Eluxadoline or its salts I APR / 17
Elvitegravir or its salts or derivatives I DEC / 18
Emamectin or its salts

including but not limited to emamectin benzoate

I DEC / 13
Embutramide I DEC / 13
Emedastine or its salts I DEC / 13
Emicizumab I OCT / 18
Empagliflozin I OCT / 15
Emtricitabine I DEC / 13
Emylcamate I DEC / 13
Enalapril or its salts or derivatives

including but not limited to enalapril maleate

I DEC / 13
Enasidenib or its salts I MAR / 19
Encephalitis vaccine (Japanese) I FEB / 02
Enflurane I DEC / 13
Enfuvirtide I DEC / 13
Enoxaparin or its salts I DEC / 13
Enrofloxacin I DEC / 13
Entacapone I DEC / 13
Entecavir I DEC / 13
Entrectinib or its salts I JUL / 20
Enzalutamide I DEC / 13
Ephedrine and its salts

in preparations containing more than 8 mg per unit dose, or with a label recommending more than 8 mg/dose or 32 mg/day, or labelled or implied for use exceeding 7 days, or if indicated for other than nasal congestion.

I FEB / 02
Ephedrine and its salts in combination products in preparations containing no more than 8 mg per unit dose, with a label recommending no more than 8 mg/dose or 32 mg/day and for use not more than 7 days, and indicated for nasal congestion. III APR / 06
Ephedrine and its salts in single entity products. in preparations containing no more than 8 mg per unit dose, with a label recommending no more than 8 mg/dose or 32 mg/day and for use not more than 7 days, and indicated for nasal congestion. II APR / 06
Epinephrine and its salts in pre-filled syringes intended for emergency administration by injection in the event of anaphylactic reactions to allergens II SEP / 99
Epinephrine and its salts. other than in pre-filled syringes intended for emergency administration by injection in the event of anaphylactic reactions to allergens I SEP / 99
Epirubicine or its salts I DEC / 13
Eplerenone I DEC / 13
Eprosartan or its salts or derivatives I DEC / 13
Epsiprantel I DEC / 13
Eptifibatide or its salts I DEC / 13
Erdafitinib or its salts I NOV / 19
Erenumab I OCT / 18
Ergot alkaloids or their salts

for human use

I DEC / 13
Eribulin or its salts or derivatives

including but not limited to eribulin mesylate

I DEC / 13
Erlotinib or its salts I DEC / 13
Ertugliflozin or its derivatives I JUL / 18
Erythrityl tetranitrate I SEP / 98
Erythromycin or its salts or derivatives

Including but not limited to: azithromycin, clarithromycin, gamithromycin, telithromycin, tulathromycin

I DEC / 18
Erythropoiesis stimulating hormone

including but not limited to erythropoietin, darbepoetin alpha, epoetin alfa

I DEC / 13
Escitalopram or its salts I DEC / 13
Esdepallethrin/piperonyl butoxide II SEP / 98
Eslicarbazepine acetate I AUG / 14
Esmolol or its salts I DEC / 13
Esomeprazole or its salts

for veterinary use

I DEC / 13
Esomeprazole or its salts

For human use, including but not limited to esomeprazole magnesium, EXCEPT when sold for the 14-day treatment for frequent heartburn at a daily dose of 20 mg, in package sizes of no more than 280 mg of esomeprazole

I NOV / 18
Esomeprazole or its salts

For human use, when sold for the 14-day treatment for frequent heartburn at a daily dose of 20 mg, in package sizes of no more than 280 mg of esomeprazole

III NOV / 18
Estramustine or its salts I DEC / 13
Etanercept I DEC / 13
Ethacrynic acid I DEC / 13
Ethambutol or its salts I DEC / 13
Ethanolamine oleate II SEP / 98
EthchlorvynolTS I SEP / 98
EthinamateTS I SEP / 98
Ethionamide or its salts I DEC / 13
Ethoheptazine and its salts II SEP / 98
Ethomoxane or its salts I DEC / 13
Ethotoin or its salts I DEC / 13
Ethyl Chloride except in trace amounts II SEP / 98
Ethyl trichloramate I DEC / 13
Ethylpapaverine and its salts I SEP / 98
Etidronic acid or its salts I DEC / 13
Etodolac or its salts or derivatives I DEC / 13
Etomidate or its salts I SEP / 20
Etoposide or its derivatives I DEC / 13
Etravirine or its salts I DEC / 13
Etretinate I DEC / 13
Etryptamine and its salts I SEP / 98
Etymemazine or its salts I DEC / 13
Evolocumab I JAN / 16
Exemestane I DEC / 13
Exenatide or its salts I DEC / 13
Ezetimibe I DEC / 13
Ezogabine or its salts or derivatives I DEC / 13

91 result(s)


Footnotes

  • C - Drug is listed in the Schedule to Part G of the Food and Drug Regulations under the Controlled Drugs and Substances Act
    N - Drug is listed in the Narcotic Control Regulations under the Controlled Drugs and Substances Act
    NR - Drug has not been reviewed by the NDSAC
    PDL - Drug is listed in the Health Canada Prescription Drug List
    TS - Drug is listed in the Benzodiazepines and Other Targeted Substances Regulations under the Controlled Drugs and Substances Act
    CR - Drug has been recommended for addition to the Controlled Drugs and Substances Act