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40-27-1
Section 40-27-1 Compact adopted; terms. The following Multistate Tax Compact is hereby approved,
adopted and enacted into law by the State of Alabama: Multistate Tax Compact Article I. Purposes.
The purposes of this compact are to: 1. Facilitate proper determination of state and local
tax liability of multistate taxpayers, including the equitable apportionment of tax bases
and settlement of apportionment disputes. 2. Promote uniformity or compatibility in significant
components of tax systems. 3. Facilitate taxpayer convenience and compliance in the filing
of tax returns and in other phases of tax administration. 4. Avoid duplicative taxation. Article
II. Definitions. As used in this compact: 1. "State" means a state of the United
States, the District of Columbia, the Commonwealth of Puerto Rico, or any territory or possession
of the United States. 2. "Subdivision" means any governmental unit or special district
of a state. 3. "Taxpayer" means any corporation, partnership, firm,...
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27-1-10.1
Section 27-1-10.1 Insurance coverage for drugs to treat life-threatening illnesses. (a) The
Legislature finds and declares the following: (1) The citizens of this state rely upon health
insurance to cover the cost of obtaining health care and it is essential that the citizens'
expectation that their health care costs will be paid by their insurance policies is not disappointed
and that they obtain the coverage necessary and appropriate for their care within the terms
of their insurance policies. (2) Some insurers deny payment for drugs that have been approved
by the Federal Food and Drug Administration, hereafter referred to as FDA, when the drugs
are used for indications other than those stated in the labelling approved by the FDA, off-label
use, while other insurers with similar coverage terms do pay for off-label use. (3) Denial
of payment for off-label use can interrupt or effectively deny access to necessary and appropriate
treatment for a person being treated for a...
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7-9A-523
Section 7-9A-523 Information from filing office; sale or license of records. (a) Acknowledgment
of filing written record. If a person that files a written record requests an acknowledgment
of the filing, the filing office shall send to the person an image of the record showing the
number assigned to the record pursuant to Section 7-9A-519(a)(1) and the date and time of
the filing of the record. However, if the person furnishes a copy of the record to the filing
office, the filing office may instead: (1) note upon the copy the number assigned to the record
pursuant to Section 7-9A-519(a)(1) and the date and time of the filing of the record; and
(2) send the copy to the person. (b) Acknowledgment of filing other record. If a person files
a record other than a written record, the filing office shall communicate to the person an
acknowledgment that provides: (1) the information in the record; (2) the number assigned to
the record pursuant to Section 7-9A-519(a)(1); and (3) the date and...
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34-23-9
Section 34-23-9 Purity of drugs dispensed. No person shall compound or sell or offer for sale
or cause to be compounded, sold, or offered for sale any medicine, drug, poison, chemical,
or pharmaceutical preparation that is adulterated. Any one of the above-named substances shall
be deemed to be adulterated if it is sold by a name recognized in the United States Pharmacopoeia
or National Formulary and it differs from the standard of strength, quality, or purity as
determined by the test laid down therein. A product may be of a lesser strength only if the
product is clearly labeled with the actual strength. The board may use product analysis data
from any laboratory that satisfies all of the following qualifications: (1) Is registered
by the Food and Drug Administration. (2) If the product is a legend controlled drug, is licensed
by the Bureau of Narcotics and Dangerous Drugs. (3) Is ISO 17025 certified. (Acts 1966, Ex.
Sess., No. 205, p. 231, §17; Act 2017-422, §1.)...
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25-7-14
Section 25-7-14 Adoption and use of labels or devices by unions or associations of workingmen.
Any union or association of workingmen may adopt and use a label or device for the purpose
of designating and distinguishing any goods, wares, or merchandise or other product of the
labor of the association or union of workingmen or of a member or members of the association
or union. A copy of any such label or device may be filed in the office of the Secretary of
State upon payment of a fee of $1.00. (Code 1907, §4876; Code 1923, §8990; Code 1940, T.
26, §330.)...
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34-24-290
Section 34-24-290 Definitions. For the purposes of this article, the following words and phrases
shall have the following meanings: (1) APPROVED PROGRAM. A program for the education and training
of assistants to physicians which has been formally approved in writing by the board. (2)
ASSISTANT TO PHYSICIAN. A person who is a graduate of an approved program, is licensed by
the board, and is registered by the board to perform medical services under the supervision
of a physician approved by the board to supervise the assistant. (3) BOARD. The Board of Medical
Examiners of the State of Alabama. (4) LEGEND DRUG. Any drug, medicine, chemical, or poison,
bearing on the label the words, "Caution, Federal Law prohibits dispensing without prescription"
or similar words indicating that the drug, medicine, chemical, or poison may be sold or dispensed
only upon the prescription of a licensed medical practitioner, except that the term legend
drug shall not include any drug, substance, or compound...
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22-6-122
Section 22-6-122 Medicaid Pharmacy and Therapeutics Committee - Classification and recommendation
of drugs; assurance of quality patient care; review of pharmaceutical products. (a) The Medicaid
Pharmacy and Therapeutics Committee shall review and recommend classes of drugs to the Medicaid
Commissioner for inclusion in the Medicaid Preferred Drug Plan. Class means a therapeutic
group of pharmaceutical agents approved by the FDA as defined by the American Hospital Formulary
Service. The classes of anti-retroviral and anti-psychotic drugs shall not be included in
the Medicaid Preferred Drug Plan. (b) The Medicaid Pharmacy and Therapeutics Committee shall
develop its preferred drug list recommendations by considering the clinical efficacy, safety,
and cost effectiveness of a product. Within each covered class, the committee shall review
and recommend drugs to the Medicaid Commissioner for inclusion on a preferred drug list. Generics
and over the counter drugs covered by Medicaid may be...
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34-23-156
Section 34-23-156 Compounding procedures. The board shall establish written procedures for
the compounding of drug products to assure that the finished products have the identity, strength,
quality, and purity they purport to have or are represented to possess. The procedures shall
include, but not be limited to, a listing of the components, their amounts in weight or volume,
the lot number of the components, if available, the order of component mixing, a description
of the compounding process, and a designated name for the finished product. The procedures
shall be followed in the execution of the compounding procedure. Components shall be accurately
weighed, measured, or subdivided, as appropriate. The operations shall be checked and rechecked
by the compounding pharmacist at each stage of the process to ensure that each weight and
measure is correct as stated in the written compounding procedures. Pharmacists shall determine
that all finished products have an acceptable degree of...
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34-23-32
Section 34-23-32 Manufacturer, bottler, packager, repackager, etc., of drugs. (a) Commencing
on August 1, 2017, every manufacturer, bottler, packager, repackager, third party logistic
provider, wholesale drug distributor, private label distributor, outsourcing facility, or
pharmacy business identified in the supply chain of drugs, medicines, chemicals, or poisons
for medicinal purposes shall register annually with the board by application for a permit
on a form furnished by the board and accompanied by a fee to be determined by the board as
follows: (1) The fee shall not be less than five hundred dollars ($500) nor more than two
thousand dollars ($2,000) for a new establishment. (2) The fee shall not be less than two
hundred fifty dollars ($250) nor more than one thousand dollars ($1,000) for a renewal permit.
(3) The fee shall not be less than five hundred dollars ($500) nor more than two thousand
dollars ($2,000) for a permit due to transfer of ownership. (b) A holder of a permit...
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22-20A-30
Section 22-20A-30 Definitions. For purposes of this article, the following terms shall have
the following meanings, respectively, unless the context otherwise requires: (1) BOARD. The
State Board of Health as defined in Section 22-2-3. (2) CATFISH. Any species of fish classified
within the family Ictaluridae. (3) DEPARTMENT. The State Department of Public Health. (4)
FOOD SERVICE ESTABLISHMENT. Any place, vehicle, or vessel where food for individual portion
service is prepared, stored, held, transported, served, or dispensed and includes any such
place regardless of whether consumption is on or off premises and which is regulated by the
Alabama Department of Public Health. (5) LABEL. A legible display of written, printed, or
graphic information on a placard, menu, sign, or other material that represents the product
to the consumer. (6) PRODUCT. Any catfish product capable of use as human food which is made
wholly or in part from any catfish or portion thereof, except products which...
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