National Association of Pharmacy Regulatory Authorities
National Association of Pharmacy Regulatory Authorities

Search: National Drug Schedules

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Drug Name Comment Schedule Date
Haemophilus influenzae type B vaccine II DEC / 98
Halazepam and its saltsTS I SEP / 98
Halofantrine and its saltsF1 I SEP / 98
Halofuginone or its saltsPDL

for veterinary use

 I MAY / 18
HaloperidolF1 I SEP / 98
Haloprogin III SEP / 98
HalothaneF1 I SEP / 98
HaloxazolamTS I JUN / 02
HeminPDL I AUG / 18
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
HeptabarbitalC2 I JUN / 02
Hetastarch and its derivativesF1 I SEP / 06
Hexachlorophene and its saltsF1 I SEP / 98
Hexacyclonate sodiumF1 I SEP / 98
Hexamethonium and its saltsF1 I SEP / 98
HexethalC2 I JUN / 02
HexobarbitalC2 I JUN / 02
Histamine and its salts except for topical use II SEP / 98
Histrelin and its saltsF1 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 insulinD II SEP / 98
Hyaluronic acid and its saltsF1 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 saltsF1 I SEP / 98
HydrocodoneN 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
HydromorphinolN I JUN / 02
HydromorphoneN I JUN / 02
Hydroquinone or its derivativesPDL

When sold in a concentration greater than 2% in preparations for topical use on the skin.

 I JUN / 19
Hydroquinone or its derivatives

When sold in a concentration less than or equal to 2% in preparations for topical use on the skin

 II JUN / 19
Hydroxocobalamin or its saltsPDL

when recommended as an antidote for cyanide poisoning

 I DEC / 13
Hydroxychloroquine and its saltsF1 I SEP / 98
4- Hydroxycoumarin or its derivativesPDL

including but not limited to acenocoumarol when sold or recommended as anticoagulants

 I DEC / 13
Hydroxyephedrine and its salts II SEP / 98
HydroxypethidineN I JUN / 02
HydroxyureaF1 I SEP / 98
Hydroxyzine or its salts or derivativesPDL

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 butylbromidePDL

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 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