British Columbia Gazette Part II — B.C. Reg. 045/2009
B.C. Reg. 045/2009
British Columbia — Gazette
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Volume 52, No. 5
B.C. Reg. 45/2009
The British Columbia Gazette,
Part II
March 10, 2009
B.C. Reg. 45/2009 , deposited March 2, 2009, pursuant
to the PHARMACISTS, PHARMACY OPERATIONS AND DRUG SCHEDULING ACT
[Section 64]. Order in Council 120/2009, approved and ordered February 27, 2009.
On the recommendation of the undersigned, the Administrator,
by and with the advice and consent of the Executive Council, orders that the
amendments to the Drug Schedules Regulation, B.C. Reg. 9/98, set out in the
schedule to the attached resolution of the Council of the College of Pharmacists
of British Columbia dated June 26, 2008, are approved.
— G. ABBOTT, Minister of Health Services ; S. BOND, Presiding Member
of the Executive Council .
Resolution of the Council of the College of Pharmacists of
British Columbia ("the Council"), made at Vancouver, British Columbia, the 26th
day of June 2008.
RESOLVED THAT:
In accordance with the authority established in
Section 64
of The Pharmacists, Pharmacy Operations and Drug Scheduling Act , R.S.B.C.
1996, c. 363 of British Columbia, the Council amends the Drug Schedules
Regulation as set out in the attached schedule, subject to the approval of the
Lieutenant Governor in Council. — Certified a true copy, Marshall Moleschi,
B.Sc. (Pharm), MHA, Registrar.
Schedule
That the Drug Schedules Regulation be amended by the:
Deletion of:
Benzoyl peroxide (preparations of 5% or less as a single ingredient)
Diclofenac and its salts
Famotidine and its salts (when sold in concentrations of 20 mg or
less per oral dosage unit and indicated for the treatment of heartburn, in
package sizes containing more than 600 mg of famotidine)
Levonorgestrel (when sold in concentrations of 0.75 mg per oral
dosage unit, packaged and labelled for emergency contraception)
and the addition of:
Abatacept
Calcium salts when sold for the treatment of hyperphosphatemiav
Deracoxib
Diclofenac and its salts, except when sold as a single medicinal
ingredient in a concentration
equivalent of 1% or less diclofenac in preparations for topical use on the
skin
Diclofenac diethylamine (in preparations for topical use on the skin in
concentrations of not more
than 1% diclofenac)
Entecavir
Erlotinib and its salts
Famotidine and its salts (when sold in concentrations of 20 mg or less per
oral dosage unit and
indicated for the treatment of heartburn, in package sizes containing more
than 600 mg of
famotidine)
Histrelin and its salts
Lanthanum salts (when sold for the treatment of hyperphosphatemia)
Levonorgestrel when sold in concentrations of 0.75 mg per oral dosage unit
(except when labelled
to be taken as a single dose of 1.5 mg and in package sizes containing no
more than 1.5 mg
levonorgestrel, packaged and labelled for emergency contraception)
Levonorgestrel (when sold in concentrations of 0.75 mg per oral dosage
unit to be taken as a single
dose of 1.5 mg, packaged and labelled for emergency contraception, in
package sizes containing no
more than 1.5 mg of levonorgestrel)
Lutropin alfa
Pregabalin and its salts and derivatives
Resocortol and its derivatives
Solifenacin and its salts
Sunitinib and its salts
Trospium chloride
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