National Drug Schedules

NOTE - Effective December 19, 2013, Schedule F to the Food and Drug Regulationswas repealed and replaced by a list of prescription drugs, called the Prescription Drug List. Therefore, all entries in the National Drug Schedules (NDS) whose footnote indicates that they appear in Schedule F (F1/F2) should now be considered part of the Prescription Drug List (PDL).

Entries whose footnote indicates that they are "Schedule F Recommended" (FR) should now be considered recommended for addition to the PDL. Some of the "Schedule F Recommended" entries may have been added or will shortly be added to the PDL by Health Canada, but either way these entries will continue to be listed in Schedule I of the NDS.

For more information on the Prescription Drug List, please consult the Health Canada website.

Drug Product Database
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Drug Name	Comment	Schedule	Date
Haemophilus influenzae type B vaccine		II	DEC / 98
Halazepam and its salts^TS		I	SEP / 98
Halofantrine and its salts^F1		I	SEP / 98
Halofuginone or its salts^PDL	for veterinary use	I	MAY / 18
Haloperidol^F1		I	SEP / 98
Haloprogin		III	SEP / 98
Halothane^F1		I	SEP / 98
Haloxazolam^TS		I	JUN / 02
Heparin and its salts	for topical use	III	SEP / 98
Heparin and its salts.	except for topical use	II	SEP / 99
Hepatitis A vaccine		I	FEB / 02
Hepatitis B Adult vaccine		I	FEB / 02
Hepatitis B Pediatric vaccine		II	DEC / 98
Hepatitis B immune globulin		I	FEB / 02
Heptabarbital^C2		I	JUN / 02
Hetastarch and its derivatives^F1		I	SEP / 06
Hexachlorophene and its salts^F1		I	SEP / 98
Hexacyclonate sodium^F1		I	SEP / 98
Hexamethonium and its salts^F1		I	SEP / 98
Hexethal^C2		I	JUN / 02
Hexobarbital^C2		I	JUN / 02
Histamine and its salts	except for topical use	II	SEP / 98
Histrelin and its salts^F1		I	OCT / 07
Homatropine and its salts	for oral use in concentrations of 2 mg or less per dosage unit	II	SEP / 98
Homatropine and its salts	for ophthalmic or parenteral use or in preparations for oral use containing more than 2 mg per dosage unit	I	SEP / 98
Human insulin^D		II	SEP / 98
Hyaluronic acid and its salts^F1	when sold or recommended for administration by intra-articular injection to horses	I	SEP / 98
Hyaluronic acid and its salts	preparations in concentrations of 5% or more	II	SEP / 98
Hyaluronidase		II	SEP / 98
Hydralazine and its salts^F1		I	SEP / 98
Hydrocodone^N		I	JUN / 02
Hydrocortisone or hydrocortisone acetate	when sold in a concentration that provides 1% or less hydrocortisone in preparations for topical use on the skin in children under 2 years of age	I	DEC / 14
Hydrocortisone or hydrocortisone acetate.	when sold in a concentration that provides 1% or less hydrocortisone in preparations for topical use on the skin in adults and children 2 years of age and over in package sizes containing more than 30 g	I	DEC / 14
Hydrocortisone or hydrocortisone acetate..	when sold in a concentration that provides 1% or less hydrocortisone in preparations for topical use on the skin in adults and children 2 years of age and over in package sizes containing no more than 30 g	III	DEC / 14
Hydromorphinol^N		I	JUN / 02
Hydromorphone^N		I	JUN / 02
Hydroquinone	topical preparations	II	SEP / 99
Hydroxocobalamin or its salts^PDL	when recommended as an antidote for cyanide poisoning	I	DEC / 13
Hydroxychloroquine and its salts^F1		I	SEP / 98
4- Hydroxycoumarin or its derivatives^PDL	including but not limited to acenocoumarol when sold or recommended as anticoagulants	I	DEC / 13
Hydroxyephedrine and its salts		II	SEP / 98
Hydroxypethidine^N		I	JUN / 02
Hydroxyurea^F1		I	SEP / 98
Hydroxyzine or its salts or derivatives^PDL	including but not limited to cetirizine and hydroxyzine hydrochloride except cetirizine or its salts when sold in concentration greater than 8.5 milligrams cetirizine per unit dose	I	DEC / 13
Hyoscine and its salts and derivatives [scopolamine]	except Hyoscine butylbromide, when recommended for parenteral use	II	AUG / 16
Hyoscine butylbromide^PDL	when recommended for parenteral use	I	AUG / 16
Hyoscyamine and its salts and derivatives	except for topical use	II	SEP / 98

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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 Drus 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

National Drug Schedules

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Footnotes