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34-23-151
Section 34-23-151 Continuing education; technician assistance; duties of pharmacist. (a) Any
pharmacist who engages in drug compounding shall be proficient in compounding and shall continually
expand his or her compounding knowledge by participating in seminars or studying appropriate
literature, or both. (b) Pharmacy technicians may assist pharmacists in the preparation of
compounds. When a written procedure for a compound is not on file at the pharmacy, a pharmacist
must direct the preparation of the compound. At all times, a pharmacist shall verify the weight
or volume of all active ingredients of a compound. While compounding, there shall be no more
than three technicians per pharmacist. (c) A pharmacist shall have responsibility to do all
of the following: (1) Verify all prescriptions. (2) Approve or reject all components of the
compounded product, drug product containers, closures, and labeling. (3) Prepare and review
all compounding records to assure that no errors have occurred...
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34-23-150
Section 34-23-150 Definitions. As used in this article, the following terms shall have the
following meanings: (1) BOARD. The Alabama State Board of Pharmacy. (2) COMPONENT. Any ingredient
used in the compounding of a drug product. (3) COMPOUNDING. The preparation, mixing, assembling,
packaging, and labeling of a drug or device as the result of a licensed practitioner's prescription
drug order or initiative based on the practitioner/patient/pharmacist relationship in the
course of professional practice. a. Compounding may also be for the purpose of, or as incident
to, research, teaching, or chemical analysis. b. Compounding includes the preparation of drugs
or devices in anticipation of prescription drug orders based on routine, regularly observed
prescribing patterns. c. Reconstitution of commercial products is not considered compounding
for purposes of this article. (4) COMPOUNDED OVER THE COUNTER (OTC) PRODUCTS. A medical product
that is prepared, packaged, and labeled in a pharmacy...
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20-2-190
Section 20-2-190 Penalties; sale of ephedrine, etc.; Alabama Drug Abuse Task Force. (a) Any
person who manufactures, sells, transfers, receives, or possesses a listed precursor chemical
violates this article if the person: (1) Knowingly fails to comply with the reporting requirements
of this article; (2) Knowingly makes a false statement in a report or record required by this
article or the rules adopted thereunder; (3) Is required by this article to have a listed
precursor chemical license or permit, and is a person as defined by this article, and knowingly
or deliberately fails to obtain such a license or permit. An offense under this subsection
shall constitute a Class C felony. (b) Notwithstanding the provisions of Section 20-2-188,
a person who possesses, sells, transfers, or otherwise furnishes or attempts to solicit another
or conspires to possess, sell, transfer, or otherwise furnish a listed precursor chemical
or a product containing a precursor chemical or ephedrine or...
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34-23-1
Section 34-23-1 Definitions. For the purpose of this chapter, the following words and phrases
shall have the following meanings: (1) ASSOCIATION. The Alabama Pharmacy Association. (2)
BIOLOGICAL PRODUCT. Has the same meaning as the term as defined in 42 U.S.C. §262. (3) BOARD
or STATE BOARD. The Alabama State Board of Pharmacy. (4) CHEMICAL. Any substance of a medicinal
nature, whether simple or compound, obtained through the process of the science and art of
chemistry, whether of organic or inorganic origin. (5) DISPENSE. To sell, distribute, administer,
leave with, give away, dispose of, deliver, or supply a drug or medicine to the ultimate user
or his or her agent. (6) DRUGS. All medicinal substances, preparations, and devices recognized
by the United States Pharmacopoeia and National Formulary, or any revision thereof, and all
substances and preparations intended for external and internal use in the cure, diagnosis,
mitigation, treatment, or prevention of disease in man or animal...
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15-18-82.1
Section 15-18-82.1 Methods of execution; election of method; constitutionality. (a) A death
sentence shall be executed by lethal injection, unless the person sentenced to death affirmatively
elects to be executed by electrocution or nitrogen hypoxia. The sentence shall be executed
pursuant to Section 15-18-82. (b) A person convicted and sentenced to death for a capital
crime at any time shall have one opportunity to elect that his or her death sentence be executed
by electrocution or nitrogen hypoxia. (1) The election for death by electrocution is waived
unless it is personally made by the person in writing and delivered to the warden of the correctional
facility within 30 days after the certificate of judgment pursuant to a decision by the Alabama
Supreme Court affirming the sentence of death or, if a certificate of judgment is issued before
July 1, 2002, the election must be made and delivered to the warden within 30 days after July
1, 2002. If a warrant of execution is pending on...
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34-23-159
Section 34-23-159 Preparation of compounded drug products for over the counter sale. A pharmacy
may prepare a compounded drug product to be sold over the counter without a prescription order.
The product shall not contain an ingredient which exceeds recommended strengths and doses
for over the counter drugs. The finished product shall not be one for which a prescription
is required. It shall be properly labeled with the product's name, directions for use, list
of active ingredients, and any necessary warnings. A compounded product shall be sold directly
to the patient after professional interaction or consultation between the pharmacist and the
patient. The product may be prepared in advance in reasonable amounts in anticipation of estimated
needs. The product shall be stored within the prescription department. The product may not
be sold in bulk to other pharmacies or vendors for resale. (Act 2003-389, p. 1094, §10; Act
2017-422, §1)...
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34-23-160
Section 34-23-160 Preparation of compounded drug products for prescriber's office use; labeling.
(a) A pharmacy may prepare a compounded drug product for a prescriber's office use. An order
by a prescriber indicating the formula and quantity ordered shall be filed in the pharmacy.
The product shall be administered in the prescriber's office and shall not be dispensed to
the patient. A record of the compounded drug product may be kept as a prescription record
in the computer of the pharmacy. A label may be generated and a number assigned by the computer
of the pharmacy for the compounded product. A record of the product's written procedure shall
be on file in the pharmacy as provided in Section 34-23-158. A record of the product's sale
to the prescriber shall remain on file at the pharmacy for not less than one year. The record
shall contain the following information: (1) The name and address of the prescriber. (2) The
date of sale. (3) A description and amount of the product sold. (b)...
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34-23-157
Section 34-23-157 Components transferred to nonoriginal container; advance product preparation;
labeling. (a) If a component is transferred from the original container to another container,
including, but not limited to, a powder being taken from the original container and stored
in another container, the new container shall be identified with the following information:
(1) Component name and supplier. (2) Lot number and expiration date, if available. (3) Strength
and concentration. (b) Products prepared in anticipation of a prescription prior to receiving
a valid prescription shall be prepared in reasonable amounts. Products shall be labeled or
documentation referenced with all of the following information: (1) A complete list of ingredients
or designated name of the preparation. (2) Preparation date. (3) Beyond use date. (4) Storage
under conditions dictated by composition and stability, including storage in a clean, dry
place or in the refrigerator. (5) Batch or lot number. (c) Upon...
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34-23-153
Section 34-23-153 Use, maintenance, and inspection of compounding equipment. Equipment used
in the compounding of drug products shall be of appropriate design and capacity, as well as
suitably located to facilitate operations for its intended use, cleaning, and maintenance.
Compounding equipment shall be of suitable composition so the surfaces that contact components
shall not be reactive, additive, or absorptive so as to alter the purity of the product compounded.
Equipment and utensils used for compounding shall be cleaned and sanitized prior to use to
prevent contamination. Equipment and utensils shall be stored in a manner to protect from
contamination. Automated, mechanical, electronic, limited commercial scale manufacturing,
or testing equipment and other types of equipment may be used in the compounding of drug products.
If such equipment is used, it shall be routinely inspected, calibrated, if necessary, or checked
to ensure proper performance. Immediately prior to the...
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34-23-11
Section 34-23-11 Physicians, dentists, registered nurses, etc., exempt from chapter. (a) Nothing
contained in this chapter shall prevent any licensed practitioner of the healing arts from
personally compounding, dispensing, administering, or supplying to his or her patient drugs
and medicines for their use. This chapter shall not apply to the manufacture or sale at wholesale
or retail of patent or proprietary medicines as purchased from a manufacturer or wholesaler,
or to the manufacture or sale at wholesale or retail of packaged, bottled, or nonbulk chemicals,
medicines, medical and dental supplies, cosmetics, and dietary foods when identified by and
sold under a trademark, trade name, or other trade symbol, privately owned or registered in
the United States Patent Office, sold or offered to be sold to the general public, if the
article meets the requirements of the Federal Food, Drug, and Cosmetic Act other than prescription
legend drugs. (b) A registered nurse in the employment of...
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