Okla. Stat. tit. 63, § 63-2-201

This is the official text of Okla. Stat. tit. 63, § 63-2-201, part of Oklahoma’s Stat. tit. 63, — part of the compiled statutory law of Oklahoma, published by the state as "Stat. tit. 63,." Browse the sections below, each linked to its official government source.

Not legal advice. This page reproduces the official text of a government statute for reference only. Laws change, and how a statute applies depends on your specific facts. For advice about your situation, consult a licensed attorney in your state.

Authority to control - Recommendations

Official statutory text

Oklahoma Statutes - Title 63. Public Health and Safety Page 904

A. The Director shall administer the provisions of this act

except as otherwise provided.

B. The Board of Pharmacy by rule may classify new products

determined to have a potential for abuse as controlled dangerous

substances after notice and hearing; provided that such rule shall

be submitted to the next regular session of the Legislature, and

such rule shall remain in force and effect unless a concurrent

resolution of disapproval is passed. Hearings shall be conducted by

the Board of Pharmacy or such officers, agents or employees as the

Board of Pharmacy may designate for the purpose. The Board of

Pharmacy shall give appropriate notice of the proposed

classification and of the time and place for a hearing. The rule so

promulgated shall become effective on a date fixed by the Board of

Pharmacy. Such rule may be amended or repealed in the same manner

as provided for its adoption. Proceedings pursuant to this

subsection shall be governed by the Administrative Procedures Act.

A new substance controlled pursuant to this subsection shall be

subject to the same regulatory provisions of this act applicable to

the Schedule of substances to which it is classified.

C. The Director may recommend to the Legislature the addition,

deletion or rescheduling of a substance.

D. In considering whether to make a recommendation or issue an

order under this section, the Director or the Board of Pharmacy, as

the case may be, shall consider the following:

1. Its actual or relative potential for abuse;

2. Scientific evidence of its pharmacological effect, if known;

3. State of current scientific knowledge regarding the

substance;

4. Its history and current pattern of abuse;

5. The scope, duration, and significance of abuse;

6. What, if any, risk there is to the public health;

7. Its psychic or physiological dependence liability; and

8. Whether the substance is an immediate precursor or principal

compound of a substance already controlled under this article.

E. Substances which are precursors of a controlled precursor

shall not be subject to control solely because they are precursors

of the controlled precursor.

F. In addition to the filing requirements of the Administrative

Procedures Act, copies of orders issued under this section shall,

during the time the Legislature is not in session, be filed with the

Chair and Vice Chair of the State Legislative Council's Judiciary

Committee.

G. The Board of Pharmacy shall exclude any nonnarcotic

substance from a schedule if such substance may, under the Federal

Food, Drug and Cosmetic Act and the law of this state, be lawfully

sold over the counter without a prescription.

Oklahoma Statutes - Title 63. Public Health and Safety Page 905

Status: repealed · Read it on the official government site

Need a lawyer in Oklahoma?

Find a Oklahoma lawyer
About this page: Statute text is reproduced from official government publishers via the Open US Law dataset (Vaquill AI, snapshot v2026.08, CC BY 4.0). Primary legislative text like this is public domain under the government-edicts doctrine (Georgia v. Public.Resource.Org, 2020). We link every section back to its official source so you can verify it independently.