Section 30-5-25 - Permit for manufacture and packaging of drugs, medicines, distribution of prescription drugs(a) Drugs may not be manufactured, made, produced, packed, packaged or prepared within the state, except under the personal supervision of a pharmacist or other qualified person as may be approved by the board;(b) A person may not manufacture, package or prepare a drug without obtaining a permit from the board.(c) A person, who offers for sale, sells, offers for sale through the method of distribution any prescription drugs is subject to this article.(d) The application for a permit shall be made on a form to be prescribed and furnished by the board and shall be accompanied by an application fee.(e) The board shall promulgate rules on permit requirements and sanitation requirements.(f) Separate applications shall be made and separate permits issued for each place of manufacture, distribution, making, producing, packing, packaging or preparation.Added by 2013 Acts, ch. 148 (HB 2577), eff. 7/1/2013.Acts, 2010 Reg. Sess., Ch. 32.This section is set out twice. See also § 30-5-25, effective until 7/1/2013.