Drug Benefit List 2010
92:00 UNCLASSIFIED THERAPEUTIC AGENTS
92:00.00 UNCLASSIFIED THERAPEUTIC AGENTS
ABATACEPT
Limited use benefit (prior approval required).
For the treatment of:
- Rheumatoid Arthritis according to established criteria.
- Juvenile Idiopathic Arthritis.
(Please refer to Appendix A).
- 250mg/Vial Injection
- 2282097 ORENCIA BMS
ADALIMUMAB
Limited use benefit (prior approval required).
For the treatment of:
- Rheumatoid Arthritis according to established criteria.
- Psoriatic Arthritis according to established criteria.
- Ankylosing Spondylitis according to established criteria.
- Psoriasis according to established criteria.
- Crohn's disease according to established criteria.
(Please refer to Appendix A).
- 40mg/0.8mL Injection
- 9857327 HUMIRA PEN ABB
- 97799757 HUMIRA PEN ABB
- 9857326 HUMIRA PRE-FILL ABB
- 97799756 HUMIRA PRE-FILL ABB
- 40mg/Vial Injection
- 2258595 HUMIRA ABB
ALENDRONATE SODIUM
Limited use benefit (prior approval required).
For the treatment of:
- Osteoporosis in patients who are 65 years of age and over or
- Osteoporosis in patients who have documented hip, vertebral or other fractures or
- Paget's Disease or
- Osteoporosis in patients with no evidence of fracture but who have a high (>20%) 10-year fracture risk or
- Osteoporosis in patients with moderate 10-year fracture risk (10-20%) and use of systemic glucocorticoid therapy > 3 months
- 5mg Tablet
- 2248727 APO-ALENDRONATE APX
- 2233055 FOSAMAX FRS
- 2270110 GEN-ALENDRONATE GEN
- 2248251 NOVO-ALENDRONATE NOP
- 2288079 SANDOZ ALENDRONATE SDZ
- 10mg Tablet
- 2248728 APO-ALENDRONATE APX
- 2201011 FOSAMAX FRS
- 2270129 GEN-ALENDRONATE GEN
- 2247373 NOVO-ALENDRONATE NOP
- 2288087 SANDOZ ALENDRONATE SDZ
ALENDRONATE SODIUM
Limited use benefit (prior approval required).
For the treatment of:
- Osteoporosis in patients who are 65 years of age and over or
- Osteoporosis in patients who have documented hip, vertebral or other fractures or
- Paget's Disease or
- Osteoporosis in patients with no evidence of fracture but who have a high (>20%) 10-year fracture risk or
- Osteoporosis in patients with moderate 10-year fracture risk (10-20%) and use of systemic glucocorticoid therapy > 3 months
- 40mg Tablet
- 2258102 CO ALENDRONATE COB
- 2201038 FOSAMAX FRS
- 70mg Tablet
- 2303078 ALENDRONATE-70 PDL
- 2248730 APO-ALENDRONATE APX
- 2258110 CO ALENDRONATE COB
- 2245329 FOSAMAX FRS
- 2286335 GEN-ALENDRONATE GEN
- 2261715 NOVO-ALENDRONATE NOP
- 2299712 PHL-ALENDRONATE PMI
- 2273179 PMS-ALENDRONATE PMS
- 2284006 PMS-ALENDRONATE FC PMS
- 2275279 RATIO-ALENDRONATE RPH
- 2270889 RIVA-ALENDRONATE RIV
- 2288109 SANDOZ ALENDRONATE SDZ
- 2302004 ZYM-ALENDRONATE ZYM
ALENDRONATE SODIUM, VITAMIN D3
Limited use benefit (prior approval required).
For the treatment of:
- Osteoporosis in patients who are 65 years of age and over or
- Osteoporosis in patients who have documented hip, vertebral or other fractures or
- Paget's Disease or
- Osteoporosis in patients with no evidence of fracture but who have a high (>20%) 10-year fracture risk or
- Osteoporosis in patients with moderate 10-year fracture risk (10-20%) and use of systemic glucocorticoid therapy > 3 months
- 70mg/2800U Tablet
- 2276429 FOSAVANCE FRS
- 70mg/5600U Tablet
- 2314940 FOSAVANCE MSP
ALFUZOSIN HYDROCHLORIDE
- 10mg Sustained Release Tablet
- 2315866 APO-ALFUZOSIN ER APX
- 2304678 SANDOZ ALFUZOSIN SDZ
- 2245565 XATRAL SAC
ALLOPURINOL
- 100mg Tablet
- 449687 ALLOPRIN VAE
- 555681 ALLOPURINOL PDL
- 402818 APO-ALLOPURINOL APX
- 364282 NOVO-PUROL NOP
- 200mg Tablet
- 514209 ALLOPRIN VAE
- 2130157 ALLOPURINOL PDL
- 479799 APO-ALLOPURINOL APX
- 565342 NOVO-PUROL NOP
- 300mg Tablet
- 454354 ALLOPRIN VAE
- 555703 ALLOPURINOL PDL
- 402796 APO-ALLOPURINOL APX
- 363693 NOVO-PUROL NOP
- 294322 ZYLOPRIM GSK
AZATHIOPRINE
- 50mg Tablet
- 2242907 APO-AZATHIOPRINE APX
- 4596 IMURAN GSK
- 2248843 NU-AZATHIOPRINE NXP
BETAHISTINE HCL
- 16mg Tablet
- 2280191 NOVO-BETAHISTINE NOP
- 2243878 SERC SPH
- 24mg Tablet
- 2280205 NOVO-BETAHISTINE NOP
- 2247998 SERC SPH
BOTULINUM TOXIN TYPE A
Limited use benefit (prior approval required).
For the treatment of:
- strabismus and blepharospasm associated with dystonia, including benign essential blepharospasm or VII nerve disorder in patients 12 years of age or older
- cervical dystonia (spasmodic torticollis)
- 100IU Injection
- 1981501 BOTOX ALL
CABERGOLINE
Limited use benefit (prior approval required).
For treatment of hyperprolactinemia in patients who have failed therapy with or are intolerant to bromocriptine.
- 0.5mg Tablet
- 2301407 CO CABERGOLINE COB
- 2242471 DOSTINEX PFI
CLOSTRIDIUM BOTULINUM NEUROTOXIN
Limited use benefit (prior approval required).
For:
- the treatment of strabismus and blepharospasm associated with dystonia, including benign essential blepharospasm or VII nerve disorder in patients 12 years of age or older or
- the treatment of cervical dystonia (spasmodic torticollis)
- 100U/vial Injection
- 2324032 XEOMIN MEZ
COLCHICINE
- 0.6mg Tablet
- 572349 COLCHICINE ODN
- 1mg Tablet
- 621374 COLCHICINE ODN
CYCLOSPORINE
Limited use benefit (prior approval required).
For transplant therapy.
- 10mg Capsule
- 2237671 NEORAL NVR
- 25mg Capsule
- 2150689 NEORAL NVR
- 2247073 SANDOZ-CYCLOSPORINE SDZ
- 50mg Capsule
- 2150662 NEORAL NVR
- 2247074 SANDOZ-CYCLOSPORINE SDZ
- 100mg Capsule
- 2150670 NEORAL NVR
- 2242821 SANDOZ-CYCLOSPORINE SDZ
- 100mg/mL Solution
- 2150697 NEORAL NVR
CYPROTERONE ACETATE, ETHINYL ESTRADIOL
- 2mg & 35mcg Tablet
- 2290308 CYESTRA-35 PMS
- 2233542 DIANE-35 BAY
- 2309556 NOVO-CYPROTERONE/ETHINYL ESTRADIOL NOP
DUTASTERIDE
Limited use benefit (prior approval required).
- For treatment of Benign Prostatic Hyperplasia (BPH) in patients who do not tolerate or have not responded to an adrenergic blocker.
or
- For use in combination therapy when monotherapy with an alpha-blocker is not sufficient.
- 0.5mg Capsule
- 2247813 AVODART GSK
ERGOCALCIFEROL
- 8288IU/mL Oral Liquid
- 80003615 ERDOL ODN
ETANERCEPT
Limited use benefit (prior approval required).
For the treatment of:
- Rheumatoid Arthritis according to established criteria.
- Psoriatic Arthritis according to established criteria.
- Ankylosing Spondylitis according to established criteria.
- Juvenile Idiopathic Arthritis
(Please refer to Appendix A).
- 25mg/Vial Injection
- 2242903 ENBREL IMX
- 50mg/mL Injection
- 2274728 ENBREL IMX
- 99100373 ENBREL SURECLICK AMG
ETIDRONATE DISODIUM
- 200mg Tablet
- 2248686 CO ETIDRONATE COB
- 1997629 DIDRONEL PGP
- 2245330 GEN-ETIDRONATE GEN
ETIDRONATE DISODIUM, CALCIUM CARBONATE
- 400mg & 500mg Tablet
- 2263866 CO-ETIDROCAL COB
- 2176017 DIDROCAL PGP
- 2247323 GEN-ETI-CAL CP GEN
- 2324199 NOVO-ETIDRONATECAL KIT NOP
EXTEMPORANEOUS MIXTURE
- Miscellaneous
- 990019 EXTEMPORANEOUS MIXTURE *
- 999994 EXTEMPORANEOUS MIXTURE *
- 999997 EXTEMPORANEOUS MIXTURE *
- 999999 EXTEMPORANEOUS MIXTURE *
- 915000 STERILE EXTEMPORANEOUS MIXTURE (QC)
FINASTERIDE
Limited use benefit (prior approval required).
- For treatment of Benign Prostatic Hyperplasia (BPH) in patients who do not tolerate or have not responded to an alpha-adrenergic blocker.
or
- For use in combination therapy when monotherapy with an alpha-blocker is not sufficient.
- 5mg Tablet
- 2348500 NOVO-FINASTERIDE NOP
- 2310112 PMS-FINASTERIDE PMS
- 2010909 PROSCAR FRS
- 2306905 RATIO-FINASTERIDE RPH
- 2322579 SANDOZ FINASTERIDE SDZ
FLUNARIZINE HCL
- 5mg Capsule
- 2246082 APO-FLUNARIZINE APX
GOLIMUMAB
Limited use benefit (prior approval required).
For the treatment of:
- Rheumatoid Arthritis according to established criteria.
- Psoriatic Arthritis according to established criteria.
- Ankylosing Spondylitis according to established criteria.
(Please refer to Appendix A).
- 50mg/0.5mL Injection
- 2324784 SIMPONI AUTO INJECTOR CER
- 2324776 SIMPONI PRE-FILLED SYRINGE CER
INFLIXIMAB
Limited use benefit (prior approval required).
For treatment of:
- Fistulizing Crohn’s disease according to established
criteria.
- For adult patients with moderately to severely active Crohn’s
Disease who have had an inadequate response to
conventional therapy.
(Please refer to Appendix A).
or
- Rheumatoid Arthritis according to established criteria
(Please refer to Appendix A).
- 100mg/Vial Injection
- 2244016 REMICADE CEN
LANREOTIDE
- 60mg/0.3mL Injection
- 2283395 SOMATULINE AUTOGEL IPS
- 90mg/0.3mL Injection
- 2283409 SOMATULINE AUTOGEL IPS
- 120mg/0.5mL Injection
- 2283417 SOMATULINE AUTOGEL IPS
LEFLUNOMIDE
Limited use benefit (prior approval required).
For treatment of patients with rheumatoid arthritis who:
- have failed treatment with methotrexate: weekly dose (PO, SC or IM) of 20mg or greater (15mg or greater if patient is 65 years of age or older) for more than 8 weeks.
- cannot tolerate or have contraindications to methotrexate.
- 10mg Tablet
- 2256495 APO-LEFLUNOMIDE APX
- 2241888 ARAVA SAC
- 2319225 GEN-LEFLUNOMIDE GEN
- 2261251 NOVO-LEFLUNOMIDE NOP
- 2288265 PMS-LEFLUNOMIDE PMS
- 2283964 SANDOZ LEFLUNOMIDE SDZ
- 20mg Tablet
- 2256509 APO-LEFLUNOMIDE APX
- 2241889 ARAVA SAC
- 2319233 GEN-LEFLUNOMIDE GEN
- 2261278 NOVO-LEFLUNOMIDE NOP
- 2288273 PMS-LEFLUNOMIDE PMS
- 2283972 SANDOZ LEFLUNOMIDE SDZ
LEUCOVORIN CALCIUM
- 5mg Tablet
- 2170493 LEUCOVORIN CALCIUM WAY
MYCOPHENOLATE MOFETIL
Limited use benefit (prior approval required).
For transplant therapy.
- 250mg Capsule
- 2192748 CELLCEPT HLR
- 500mg Tablet
- 2237484 CELLCEPT HLR
MYCOPHENOLATE SODIUM
Limited use benefit (prior approval required).
For transplant therapy.
- 180mg Enteric Coated Tablet
- 2264560 MYFORTIC NVR
- 360mg Enteric Coated Tablet
- 2264579 MYFORTIC NVR
NEDOCROMIL SODIUM
- 2% Ophth Solution
- 2241407 ALOCRIL ALL
OCTREOTIDE
- 10mg/Vial Injection
- 2239323 SANDOSTATIN LAR NVR
- 20mg/Vial Injection
- 2239324 SANDOSTATIN LAR NVR
- 30mg/Vial Injection
- 2239325 SANDOSTATIN LAR NVR
- 50mcg/mL Injection
- 2248639 OCTREOTIDE ACETATE OMEGA OMG
- 839191 SANDOSTATIN NVR
- 100mcg/mL Injection
- 2248640 OCTREOTIDE ACETATE OMEGA OMG
- 839205 SANDOSTATIN NVR
- 200mcg/mL Injection
- 2248642 OCTREOTIDE ACETATE OMEGA OMG
- 2049392 SANDOSTATIN NOV
- 500mcg/mL Injection
- 2248641 OCTREOTIDE ACETATE OMEGA OMG
- 839213 SANDOSTATIN NVR
PAMIDRONATE DISODIUM
- 30mg Injection
- 2059762 AREDIA IV NVR
- 2244550 PAMIDRONATE DISODIUM MAY
- 2264951 RHOXAL-PAMIDRONATE RHO
- 60mg Injection
- 2244551 PAMIDRONATE DISODIUM HOS
- 2264978 RHOXAL-PAMIDRONATE SDZ
PAMIDRONATE DISODIUM
- 90mg Injection
- 2059789 AREDIA IV NVR
- 2244552 PAMIDRONATE DISODIUM MAY
- 2245999 PMS-PAMIDRONATE PMS
- 2264986 RHOXAL-PAMIDRONATE SDZ
PENTOSAN POLYSULFATE SODIUM
- 100mg Capsule
- 2029448 ELMIRON JNO
RISEDRONATE SODIUM
Limited use benefit (prior approval required).
For the treatment of:
- Osteoporosis in patients who are 65 years of age and over or
- Osteoporosis in patients who have documented hip, vertebral or other fractures or
- Paget's Disease or
- Osteoporosis in patients with no evidence of fracture but who have a high (>20%) 10-year fracture risk or
- Osteoporosis in patients with moderate 10-year fracture risk (10-20%) and use of systemic glucocorticoid therapy > 3 months
- 5mg Tablet
- 2242518 ACTONEL PGP
- 2298376 NOVO-RISEDRONATE NOP
- 30mg Tablet
- 2239146 ACTONEL PGP
- 2298384 NOVO-RISEDRONATE NOP
- 35mg Tablet
- 2246896 ACTONEL PGP
- 2298392 NOVO-RISEDRONATE NOP
SIROLIMUS
Limited use benefit (prior approval required).
Coverage will be provided as a second line therapy for patients failing mycophenolate mofetil.
- 1mg/mL Oral Liquid
- 2243237 RAPAMUNE WAY
- 1mg Tablet
- 2247111 RAPAMUNE WAY
TAMSULOSIN HCL
- 0.4mg Long Acting Capsule
- 2281392 NOVO-TAMSULOSIN NOP
- 2294885 RAN-TAMSULOSIN RBY
- 2294265 RATIO-TAMSULOSIN RPH
- 2295121 SANDOZ TAMSULOSIN SDZ
- 0.4mg Long Acting Tablet
- 2270102 FLOMAX CR BOE
TAMSULOSIN HYDROCHLORIDE
- 0.4mg Sustained Release Capsule
- 2298570 GEN-TAMSULOSIN MYL
TETRABENAZINE
- 25mg Tablet
- 2199270 NITOMAN LHL
USTEKINUMAB
Limited use benefit (prior approval required).
For the treatment of moderate to severe psoriasis in patients who meet the following criteria:
- Body surface area involvement greater than 10% and/or significant involvement of the face, hands, feet or genital region and
- Intolerance or lack of response to methotrexate and cyclosporine or
- A contraindication to methotrexate and/or cyclosporine and
- Intolerance or lack of response to phototherapy or
- Inability to access phototherapy
Coverage beyond 16 weeks will be based on a significant reduction in the Body Surface Area (BSA) involved and improvements in the Psoriasis Area Severity Index (PASI) score and the Dermatology Life Quality Index (DLQI).
- 45mg/0.5mL Injection
- 2320673 STELARA JNO
WATER
- 100% Injection
- 38202 STERILE WATER * ABB
- 99002264 STERILE WATER *
- 905178 WATER FOR INJECTION *
- 905194 WATER FOR INJECTION *
- 905224 WATER FOR INJECTION *
ZOLEDRONIC ACID
Limited use benefit (prior approval required).
For the treatment of Paget’s disease. Coverage will be
granted for one dose per 12 month period.
- 5mg/100mL Injection
- 2269198 ACLASTA NOV
92:44.00
TACROLIMUS
Limited use benefit (prior approval required).
For transplant therapy.
- 0.5mg Capsule
- 2243144 PROGRAF AST
- 1mg Capsule
- 2175991 PROGRAF AST
- 5mg Capsule
- 2175983 PROGRAF AST
- 5mg/mL Injection
- 2176009 PROGRAF AST
- 0.5mg Long Acting Capsule
- 2296462 ADVAGRAF AST
- 1mg Long Acting Capsule
- 2296470 ADVAGRAF AST
- 5mg Long Acting Capsule
- 2296489 ADVAGRAF AST