Publications
Medi-Cal List of Contract Drugs
The following provider manual sections have been updated: Drugs: Contract Drugs List Part 1 – Prescription Drugs and Drugs: Contract Drugs List Part 4 – Therapeutic Classifications Drugs.
Changes, Clarification of Code I, effective immediately| Drug | Strength and/or Size | Billing Unit | |||
| * | AMPHETAMINE, MIXED SALTS | ||||
| (AMPHETAMINE SULFATE, AMPHETAMINE ASPARATE, DEXTROAMPHETAMINE SULFATE AND DEXTROAMPHETAMINE SACCHARATE) | |||||
| * | Restricted to use in Attention Deficit Disorder in individuals |
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| Tablets | 5 mg | ea | |||
| 7.5 mg | ea | ||||
| 10 mg | ea | ||||
| 12.5 mg | ea | ||||
| 15 mg | ea | ||||
| 20 mg | ea | ||||
| 30 mg | ea | ||||
| * | DEXMETHYLPHENIDATE HCL | ||||
| * | Restricted to use in Attention Deficit Disorder in individuals |
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| Capsules, extended release | 5 mg | ea | |||
| 10 mg | ea | ||||
| 15 mg | ea | ||||
| 20 mg | ea | ||||
| * | DEXTROAMPHETAMINE SULFATE | ||||
| * | Restricted to use in Attention Deficit Disorder in individuals 16 years of age only. |
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| Tablets | 5 mg | ea | |||
| 10 mg | ea | ||||
| * | LISDEXAMFETAMINE DIMESYLATE | ||||
| * | Restricted to use in Attention Deficit Disorder in individuals 16 years of age only. |
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| Capsules | 20 mg | ea | |||
| 30 mg | ea | ||||
| 40 mg | ea | ||||
| 50 mg | ea | ||||
| 60 mg | ea | ||||
| 70 mg | ea | ||||
| METHYLPHENIDATE HCL | |||||
| * | Tablets | 5 mg | ea | ||
| 10 mg | ea | ||||
| 20 mg | ea | ||||
| * | Restricted to use in Attention Deficit Disorder in individuals |
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| * | Tablets, extended release | 18 mg | ea | ||
| 27 mg | ea | ||||
| 36 mg | ea | ||||
| 54 mg | ea | ||||
| * | Restricted to use in Attention Deficit Disorders in individuals |
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| * | PEMOLINE | ||||
| * | Restricted to use in Attention Deficit Disorders in individuals |
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| Tablets or capsules | 18.75 mg | ea | |||
| 37.5 mg | ea | ||||
| 75 mg | ea | ||||
| Tablets (chewable) | 37.5 mg | ea | |||
Change, effective September 17, 2008
| Drug | Strength and/or Size | Billing Unit | |||
| ‡ | * | TIPRANAVIR | |||
| * | Restricted to use as combination therapy in the treatment of Human Immunodeficiency Virus (HIV) infection. | ||||
| Capsules | 250 mg | ea | |||
| Oral solution | 100 mg/cc | cc | |||
Changes, effective September 22, 2008
| Drug | Strength and/or Size | Billing Unit | ||
| ‡ | TOPOTECAN HCL | |||
| Capsules | 0.25 mg | ea | ||
| 1 mg | ea | |||
| Powder for injection | 4 mg /vial | ea | ||
Changes, effective November 1, 2008
| Drug | Strength and/or Size | Billing Unit | ||||
| * | ALFUZOSIN HCL | |||||
| * | Restricted to NDC labeler code 00024 (Sanofi-Aventis, US LLC) only. | |||||
| + | Tablets, extended release | 10 mg | ea | |||
| METRONIDAZOLE | ||||||
| Oral tablets | 250 mg | ea | ||||
| 500 mg | ea | |||||
| Injection | 500 mg/100 cc | cc | ||||
| Powder for injection | 500 mg vial | ea | ||||
| * | Topical gel | 0.75 % | 28.4 Gm | Gm | ||
| * | Restricted to claims submitted with dates of service from March 1, 1994 through December 31, 2005. | |||||
| * | Vaginal gel | 0.75 % | 70 Gm | Gm | ||
| * | Restricted to NDC labeler code 00089 (3M) and NDC labeler code 29336 (Graceway Pharmaceuticals, LLC) for vaginal gel only. | |||||
| OLOPATADINE HCL | ||||||
| Ophthalmic solution | 0.1 % | cc | ||||
| 0.2 % | cc | |||||
| Nasal spray | 0.6 % | Gm | ||||
| * | ZIPRASIDONE HCL | |||||
| * | Restricted to individuals 6 years of age and older and to NDC labeler code 00049 (Pfizer, Inc.) only. | |||||
| Capsules | 20 mg | ea | ||||
| 40 mg | ea | |||||
| 60 mg | ea | |||||
| 80 mg | ea | |||||
Changes, effective January 1, 2009
| Drug | Strength and/or Size | Billing Unit | |||
| * | MOMETASONE FUROATE | ||||
| * | Restricted to claims submitted with dates of service from October 1, 2005 through December 31, 2008 only. | ||||
| Oral powder for inhalation | 30 inhalations/0.24 Gm | Gm | |||
| 60 inhalations/0.24 Gm | Gm | ||||
| 120 inhalations/0.24 Gm | Gm | ||||
| ‡ | * | NORELGESTROMIN AND ETHINYL ESTRADIOL | |||
| * | Restricted to claims submitted with dates of service from March 2, 2002 through December 31, 2008 only. | ||||
| Transdermal patch | 6 mg – 0.75 mg | ea | |||
| Note: | Payment limited to a minimum dispensing quantity of three cycles except with the initial prescription or when uthorization is obtained. | ||||
| OXYBUTYNIN CHLORIDE | |||||
| + | Tablets | 5 mg | ea | ||
| * | + Tablets, extended release | 5 mg | ea | ||
| 10 mg | ea | ||||
| 15 mg | ea | ||||
| * | Restricted to NDC labeler code 17314 (Alza Corporation) and to claims submitted with dates of service from December 1, 1998 through December 31, 2008 for extended release tablets only. | ||||

