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Oklahoma Legislature· SB 1591Placed on General Order

An act relating to medical marijuana, the official text

Shown verbatim: the complete text as captured from the official PDF posted by the Oklahoma Legislature, fetched 2026-07-23. Page and line markers are part of the official record; nothing is edited or removed. The official bill page.
1                   STATE OF OKLAHOMA

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2                  2nd Session of the 60th Legislature (2026)

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3 SENATE BILL 1591                By: Rosino
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6                   AS INTRODUCED

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7   An Act relating to medical marijuana; amending 63

7   O.S. 2021, Sections 423, as last amended by Section

8   8, Chapter 182, O.S.L. 2024 and 427.18, as last

8   amended by Section 1, Chapter 272, O.S.L. 2025 (63

9   O.S. Supp. 2025, Sections 423 and 427.18), which

9   relate to medical marijuana processing license and

10  packaging and labeling requirements; limiting certain

10  tetrahydrocannabinol (THC) amounts in certain

11  products and packages; updating statutory language;

11  and providing an effective date.

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14 BE IT ENACTED BY THE PEOPLE OF THE STATE OF OKLAHOMA:
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15  SECTION 1.      AMENDATORY    63 O.S. 2021, Section 423, as last

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16 amended by Section 8, Chapter 182, O.S.L. 2024 (63 O.S. Supp. 2025,
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17 Section 423), is amended to read as follows:
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18  Section 423. A. The Oklahoma Medical Marijuana Authority shall

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19 make available on its website in an easy-to-find location an
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20 application for a medical marijuana processing license. The
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21 Authority shall be authorized to issue two types of medical
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22 marijuana processor licenses based on the level of risk posed by the
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23 type of processing conducted:
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24  1. Nonhazardous medical marijuana processor license; and

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    Req. No. 2858                                              Page 1
1   2. Hazardous medical marijuana processor license.

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2 The application fee for a nonhazardous or hazardous medical
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3 marijuana processor license shall be paid by the applicant in the
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4 amounts provided for in Section 427.14 of this title. A method of
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5 payment shall be provided on the website of the Authority. The
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6 Authority shall have ninety (90) business days to review the
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7 application; approve, reject, or deny the application; and send the
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8 approval, rejection, or denial letter stating the reasons for the
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9 rejection or denial to the applicant in the same method the
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10 application was submitted to the Authority.
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11  B. The Authority shall approve all applications which meet the

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12 following criteria:
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13  1. The applicant must be twenty-five (25) years of age or

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14 older;
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15  2. The applicant, if applying as an individual, must show

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16 residency in this state;
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17  3. All applying entities must show that all members, managers,

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18 and board members are Oklahoma residents of this state;
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19  4. An applying entity may show ownership of nonstate residents,

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20 but that percentage ownership may not exceed twenty-five percent
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21 (25%);
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22  5. All applying individuals or entities must be registered to

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23 conduct business in this state; and
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    Req. No. 2858                                              Page 2
1   6. All applicants must disclose all ownership interests in the

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2 processing operation.
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3   Applicants with a nonviolent felony conviction in the last two

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4 (2) years, any other felony conviction in the last five (5) years,
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5 inmates in the custody of the Department of Corrections or any
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6 person currently incarcerated shall not qualify for a medical
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7 marijuana processing license.
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8   C. 1. A licensed processor may take marijuana plants and

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9 distill or process these plants into concentrates, edibles, and
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10 other forms for consumption. No individual edible medical marijuana
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11 product shall include more than ten (10) milligrams of
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12 tetrahydrocannabinol (THC) per edible and no more than one hundred
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13 (100) milligrams of THC per package.
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14  2. The Executive Director of the Authority shall make available

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15 a set of standards which shall be used by licensed processors in the
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16 preparation of edible marijuana products. The standards should be
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17 in line with current food preparation guidelines. No excessive or
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18 punitive rules may be established by the Executive Director.
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19  3. Up to two times a year, the Authority may inspect a

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20 processing operation and determine its compliance with the
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21 preparation standards. If deficiencies are found, a written report
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22 of the deficiency shall be issued to the licensed processor. The
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23 licensed processor shall have one (1) month to correct the
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    Req. No. 2858                                              Page 3
1 deficiency or be subject to a fine of Five Hundred Dollars ($500.00)
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2 for each deficiency.
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3   4. A licensed processor may sell marijuana products it creates

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4 to a licensed dispensary or any other licensed processor. All sales
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5 by a licensed processor shall be considered wholesale sales and
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6 shall not be subject to taxation.
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7   5. Under no circumstances may a licensed processor sell

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8 marijuana or any marijuana product directly to a licensed medical
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9 marijuana patient or licensed caregiver. However, a licensed
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10 processor may process cannabis into a concentrated form for a
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11 licensed medical marijuana patient for a fee.
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12  6. Licensed processors shall be required to complete a monthly

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13 yield and sales report to the Authority. This report shall be due
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14 on the fifteenth of each month and shall provide reporting on the
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15 previous month. This report shall detail the amount of marijuana
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16 and medical marijuana products purchased in pounds, the amount of
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17 marijuana cooked or processed in pounds, and the amount of waste in
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18 pounds. Additionally, this report shall show total wholesale sales
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19 in dollars. The Authority shall have oversight and auditing
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20 responsibilities to ensure that all marijuana being processed is
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21 accounted for.
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22  D. The Authority shall oversee the inspection and compliance of

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23 licensed processors producing products with marijuana as an
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    Req. No. 2858                                               Page 4
1 additive. If it becomes permissible under federal law, marijuana
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2 may be moved across state lines.
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3   E. Any device used for the processing or consumption of medical

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4 marijuana shall be considered legal to be sold, manufactured,
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5 distributed, and possessed. No merchant, wholesaler, manufacturer,
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6 or individual may be unduly harassed or prosecuted for selling,
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7 manufacturing, or possessing marijuana paraphernalia.
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8   SECTION 2.      AMENDATORY      63 O.S. 2021, Section 427.18, as

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9 last amended by Section 1, Chapter 272, O.S.L. 2025 (63 O.S. Supp.
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10 2025, Section 427.18), is amended to read as follows:
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11  Section 427.18. A. A medical marijuana business shall not

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12 sell, transfer, or otherwise distribute medical marijuana or medical
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13 marijuana product that has not been packaged and labeled in
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14 accordance with this section and rules promulgated by the Executive
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15 Director of the Oklahoma Medical Marijuana Authority.
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16  B. A medical marijuana dispensary shall return medical

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17 marijuana and medical marijuana product that does not meet packaging
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18 or labeling requirements in this section or rules promulgated
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19 pursuant thereto to the entity who transferred it to the dispensary.
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20 The medical marijuana dispensary shall document to whom the item was
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21 returned, what was returned, and the date of the return, or dispose
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22 of any usable marijuana that does not meet these requirements in
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23 accordance with the Oklahoma Medical Marijuana and Patient
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24 Protection Act.
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    Req. No. 2858                                               Page 5
1   C. 1. Medical marijuana packaging shall be packaged to

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2 minimize its appeal to children and shall not depict images other
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3 than the business name logo of the medical marijuana producer and
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4 image of the product.
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5   2. A medical marijuana business shall not place any content on

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6 a container in a manner that reasonably appears to target
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7 individuals under the age of twenty-one (21) including, but not
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8 limited to, cartoon characters or similar images.
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9   3. Labels on a container shall not include any false or

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10 misleading statements.
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11  4. No container shall be intentionally or knowingly labeled so

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12 as to cause a reasonable patient confusion as to whether the medical
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13 marijuana, medical marijuana concentrate, or medical marijuana
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14 product is a trademarked product or labeled in a manner that
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15 violates any federal trademark law or regulation. The label on the
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16 container shall include a warning that states the following:
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17  a. "For use by licensed medical marijuana patients only",

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18  b. "Keep out of reach of children",

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19  c. "It is illegal to drive a motor vehicle while under

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20                 the influence of marijuana or marijuana products",

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21  d. "Women should not use marijuana or marijuana products

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22                 during pregnancy because of the risk of birth

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23                 defects", and

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24  e. "This product has been tested for contaminants".

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    Req. No. 2858                                                 Page 6
1   5. The label on the container shall not make any claims

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2 regarding health or physical benefits to the patient.
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3   6. The container itself may be clear in order to allow licensed

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4 medical marijuana patients and licensed medical marijuana caregivers
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5 the ability to view the product inside the container but shall be
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6 child-resistant, as defined in Section 427.2 of this title.
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7   7. At the point of sale and transfer of any medical marijuana,

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8 medical marijuana concentrate, or medical marijuana products to a
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9 licensed medical marijuana patient or licensed medical marijuana
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10 caregiver, the dispensary shall place the medical marijuana, medical
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11 marijuana concentrate, or medical marijuana products in an exit
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12 package, as such term is defined in Section 427.2 of this title.
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13  8. No individual edible medical marijuana product sold shall

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14 include more than ten (10) milligrams of tetrahydrocannabinol (THC)
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15 per edible and no more than one hundred (100) milligrams of THC per
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16 package.
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17  D. The Executive Director shall develop minimum standards for

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18 packaging and labeling of medical marijuana, medical marijuana
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19 concentrate, and medical marijuana products. Such standards shall
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20 include, but not be limited to, the required contents of labels to
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21 be affixed to all medical marijuana, medical marijuana concentrate,
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22 and medical marijuana products prior to transfer to a licensed
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23 patient or caregiver, which shall include, at a minimum:
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24  1. THC and other cannabinoid potency, and terpenoid potency;

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    Req. No. 2858                                              Page 7
1   2. A statement indicating that the product has been tested for

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2 contaminants;
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3   3. One or more product warnings to be determined by the

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4 Executive Director; and
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5   4. Any other information the Executive Director deems

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6 necessary.
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7   SECTION 3. This act shall become effective November 1, 2026.

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9   60-2-2858      CAD     1/13/2026 10:53:59 AM

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    Req. No. 2858                                          Page 8
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