Alabama Statutes
§ 34-23-32.2 — Adherence to FDA Guidelines in the Drug Quality and Security Act; Annual Permits; Fees
Alabama § 34-23-32.2
JurisdictionAlabama
Title 34Professions and Businesses
Ch. 23Pharmacists and Pharmacies
Art. 2Licenses and Permits
Div. 1General Provisions
This text of Alabama § 34-23-32.2 (Adherence to FDA Guidelines in the Drug Quality and Security Act; Annual Permits; Fees) is published on Counsel Stack Legal Research, covering Alabama primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.
Bluebook
Ala. Code § 34-23-32.2 (2026).
Text
(a)Any requirements established by the FDA Guidelines in the Drug Quality and Security Act shall be adhered to by the affected parties.
(b)(1) The board may issue an annual permit to any manufacturer, manufacturer affiliate, bottler, packager, repackager, third-party logistic provider, wholesale drug distributor, private label distributor, or pharmacy business identified in the supply chain of any drugs, legend drugs, medicines, chemicals, or poisons for medicinal purposes.
(2)The board, by rule, shall establish fees for the various categories of permits issued under this section of not less than five hundred dollars ($500) nor more than two thousand dollars ($2,000). In addition, the board, by rule, may establish renewal fees and late fees for failure to renew a permit in a timely manne
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Legislative History
(Act 2017-422, p. 1392, §2.; Act 2025-372, §3)
Nearby Sections
15
§ 34-1-1
Short Title§ 34-1-11
Annual Permits to Practice; Inactive Status; Continuing Education. (Amended by Act 2026-16)§ 34-1-17
Acts Not Prohibited§ 34-1-18
Injunctions Against Unlawful Acts§ 34-1-19
Misdemeanors; Penalties§ 34-1-20
Evidence of Unlawful PracticeCite This Page — Counsel Stack
Bluebook (online)
Alabama § 34-23-32.2, Counsel Stack Legal Research, https://law.counselstack.com/statute/al/34-23-32.2.