80 chapters · 1,101 sections in this title.
Conn. Gen. Stat. § 20-617a Flavoring agent added to prescription product. Exemptions.
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Sec. 20-617a. Flavoring agent added to prescription product. Exemptions. (a) For purposes of this section, “flavoring agent” means an additive used in food or drugs when such additive (1) is used in accordance with good manufacturing practice principles and in the minimum quantit…
Conn. Gen. Stat. § 20-617b Compliance packaging. Requirements. Regulations.
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Sec. 20-617b. Compliance packaging. Requirements. Regulations. (a)(1) A pharmacist or advanced pharmacy technician may, at the request of a patient, the patient's representative or the patient's prescribing practitioner, dispense to the patient compatible drugs in compliance pack…
Conn. Gen. Stat. § 20-618 (Formerly Sec. 21a-107). Repackaged drugs not considered misbranded, when.
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Sec. 20-618. (Formerly Sec. 21a-107). Repackaged drugs not considered misbranded, when. Notwithstanding the provisions of section 21a-106 concerning misbranding of drugs or devices, a drug shall not be considered misbranded when repackaged by a pharmacy or an institutional pharma…
Conn. Gen. Stat. § 20-619 (Formerly Sec. 20-185a). Substitution of generic drugs and biological products. Definitions. Interchangeable biological products. Prescribing practitioners. Pharmacy signs. Dispensing. Records. Regulations.
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Sec. 20-619. (Formerly Sec. 20-185a). Substitution of generic drugs and biological products. Definitions. Interchangeable biological products. Prescribing practitioners. Pharmacy signs. Dispensing. Records. Regulations. (a) For the purposes of section 20-579 and this section: (1)…