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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
Gabapentin or its salts or derivativesPDL I DEC / 13
Galantamine or its salts or derivativesPDL I DEC / 13
Gallamine triethiodidePDL I DEC / 13
Gallium or its saltsPDL I DEC / 13
GalsulfasePDL I DEC / 13
Gamithromuycin PDL I DEC / 13
Ganciclovir or its saltsPDL I DEC / 13
Ganirelix or its salts or derivativesPDL

Including but not limited to ganirelix acetate. 

I DEC / 13
Gatifloxacin or its salts or derivativesPDL I DEC / 13
GefitinibPDL I DEC / 13
Gemcitabine or its saltsPDL I DEC / 13
Gemfibrozil or its saltsPDL I DEC / 13
Gemifloxacin or its saltsPDL I DEC / 13
Gentamicin or its salts or derivativesPDL

Including but not limited to netilmicin.

I DEC / 13
Gentian Violet II DEC / 01
Glatiramer or its saltsPDL I DEC / 13
GlecaprevirPDL I SEP / 17
GliclazidePDL I DEC / 13
GlimepiridePDL I DEC / 13
GlipizidePDL I DEC / 13
Glucagon II SEP / 98
Glutamic acid and its salts gastric acidifiers U FEB / 99
GlutethimideC1 I SEP / 98
Glyburide or its salts or derivativesPDL I DEC / 13
Glyceroargentinate III SEP / 98
Glycopyrrolate or its salts

except glycopyrronium bromide, including but not limited to glycopyrrolate, when used orally or for inhalation

II DEC / 17
Glycopyrronium bromidePDL

Including but not limited to glycopyrrolate, when used orally or for inhalation.

I DEC / 17
Gold or its salts or derivativesPDL

Including but not limited to aurothioglucose, auranofin and sodium aurothiomalate, when sold for administration by injection.

I DEC / 13
GolimumabPDL I DEC / 13
Gonadorelin or its saltsPDL I DEC / 13
Gonadotropin releasing factor or its analoguesPDL

For veterinary use.

I DEC / 13
Gonadotropin, chorionic (human)PDL I DEC / 13
Gonadotropins, serum (human)PDL I DEC / 13
Goserelin or its saltsPDL I DEC / 13
Gramicidin and its salts for topical use U
Gramicidin and its salts and derivatives for ophthalmic use III JUN / 06
Granisetron or its saltsPDL I DEC / 13
Grapiprant or its saltsPDL

For veterinary use

I FEB / 19
GrazoprevirPDL I AUG / 16
Grepafloxacin or its salts or derivativesPDL I DEC / 13
Griseofulvin or its salts or derivativesPDL

For human use.

I DEC / 13
Guaifenesin U
Guanethidine or its saltsPDL I DEC / 13
Guanfacine or its salts or derivativesPDL I DEC / 13
GuselkumabPDL I MAR / 18

45 result(s)

Footnotes

  • C1: Drug is in the Controlled Drugs and Substances Act and Part I of the Schedule to Part G of the Food and Drug Regulations
  • C2: Drug is in the Controlled Drugs and Substances Act and Part II of the Schedule to Part G of the Food and Drug Regulations
  • C3: Drug is in the Controlled Drugs and Substances Act and Part III of the Schedule to Part G of the Food and Drug Regulations
  • C4: drug is in the Controlled Drugs and Substances Act
  • C5: drug is in the Regulations Under CDSA
  • CR: drug has been recommended for addition to the Controlled Drugs and Substances Act
  • CR-C: drug has been recommended for addition to the Controlled Drugs and Substances Act, Part G of the Food and Drug Regulations
  • CR-N: drug has been recommend for addition to the Controlled Drugs and Substances Act, Narcotic Control Regulations
  • CR-TS: drug has been recommended for addition to the Controlled Drugs and Substances Act, Benzodiazepines and Other Targeted Substances Regulations
  • F1: drug appears in Part I of Schedule F to the Food and Drugs Act and Regulations
  • F2: drug appears in Part II of Schedule F to the Food and Drugs Act and Regulations
  • FR: drug has been recommended for addition to Schedule F to the Food and Drugs Act and Regulations ("Schedule F Recommended")
  • N: drug is in the Narcotic Control Regulations under the Controlled Drugs and Substances Act
  • NR: drug has not been reviewed by NDSAC
  • PDL: drug is in the Prescription Drug List (effective Dec. 19, 2013)
  • R: drug is in Part J of the Food and Drugs Act and listed in the Controlled Drugs and Substances Act
  • TS: drug is in the Benzodiazepines and Other Targeted Substances Regulations under the Controlled Drugs and Substances Act
  • U: drug has been reviewed by NDSAC and is unscheduled