{"formats":[{"name":"JSON","format":"json","url":"\/downloads\/2026\/code-json\/54.1-3437.1.json"},{"name":"Plain Text","format":"text","url":"\/downloads\/2026\/code-text\/54.1-3437.1.txt"},{"name":"XML","format":"xml","url":"\/downloads\/2026\/code-xml\/54.1-3437.1.xml"},{"name":"HTML","format":"html","url":"\/downloads\/2026\/code-html\/54.1-3437.1.html"}],"law_id":368757,"edition_id":2,"section_id":368757,"structure_id":52542,"section_number":"54.1-3437.1","catch_line":"Limited permit for repackaging drugs","history":"1997, c. 218; 2009, cc. 813, 840.","full_text":"The Board may issue a limited manufacturing permit for the purpose of repackaging drugs, upon such terms and conditions approved by the Board, to the pharmacy directly operated by the Department of Behavioral Health and Developmental Services and which serves clients of the community services boards.\n\n","order_by":null,"text":{"0":{"id":1374292,"text":"The Board may issue a limited manufacturing permit for the purpose of repackaging drugs, upon such terms and conditions approved by the Board, to the pharmacy directly operated by the Department of Behavioral Health and Developmental Services and which serves clients of the community services boards.","type":"section","prefixes":[""],"prefix":"","entire_prefix":"","prefix_anchor":"","level":1}},"ancestry":[{"id":52542,"edition_id":2,"name":"Permitting of Manufacturers","identifier":"4","label":"article","depth":4,"order_by":5,"parent_id":52537,"metadata":{"child_laws":9,"child_structures":0},"date_created":"2026-08-02 03:00:45","date_modified":"2026-08-02 12:35:15","permalink":{"id":1470555,"object_type":"structure","relational_id":52542,"identifier":"4","token":"54.1\/III\/34\/4","url":"\/54.1\/III\/34\/4\/","edition_id":2,"permalink":0,"preferred":1}},{"id":52537,"edition_id":2,"name":"Drug Control Act","identifier":"34","label":"chapter","depth":3,"order_by":16,"parent_id":52479,"metadata":{"child_laws":127,"child_structures":10},"date_created":"2026-08-02 03:00:37","date_modified":"2026-08-02 12:35:13","permalink":{"id":1470225,"object_type":"structure","relational_id":52537,"identifier":"34","token":"54.1\/III\/34","url":"\/54.1\/III\/34\/","edition_id":2,"permalink":0,"preferred":1}},{"id":52479,"edition_id":2,"name":"Professions and Occupations Regulated by Boards Within the Department of Health Professions","identifier":"III","label":"subtitle","depth":2,"order_by":3,"parent_id":52436,"metadata":{"child_laws":738,"child_structures":83},"date_created":"2026-08-02 02:59:23","date_modified":"2026-08-02 12:35:00","permalink":{"id":1468107,"object_type":"structure","relational_id":52479,"identifier":"III","token":"54.1\/III","url":"\/54.1\/III\/","edition_id":2,"permalink":0,"preferred":1}},{"id":52436,"edition_id":2,"name":"Professions and Occupations","identifier":"54.1","label":"title","depth":1,"order_by":118,"parent_id":null,"metadata":{"child_laws":1282,"child_structures":163},"date_created":"2026-08-02 02:58:52","date_modified":"2026-08-02 12:34:51","permalink":{"id":1466315,"object_type":"structure","relational_id":52436,"identifier":"54.1","token":"54.1","url":"\/54.1\/","edition_id":2,"permalink":0,"preferred":1}}],"structure_contents":[{"id":368758,"structure_id":52542,"section_number":"54.1-3437","catch_line":"Permit to manufacture drugs","url":"\/54.1-3437\/","token":"54.1\/III\/34\/4\/54.1-3437","metadata":false},{"id":368757,"structure_id":52542,"section_number":"54.1-3437.1","catch_line":"Limited permit for repackaging drugs","url":"\/54.1-3437.1\/","token":"54.1\/III\/34\/4\/54.1-3437.1","metadata":false},{"id":368759,"structure_id":52542,"section_number":"54.1-3438","catch_line":"Manufacturing, etc., of drugs or proprietary medicines, to be supervised by pharmacist","url":"\/54.1-3438\/","token":"54.1\/III\/34\/4\/54.1-3438","metadata":false},{"id":368760,"structure_id":52542,"section_number":"54.1-3439","catch_line":"Application for nonrestricted manufacturing permit; fee","url":"\/54.1-3439\/","token":"54.1\/III\/34\/4\/54.1-3439","metadata":false},{"id":368761,"structure_id":52542,"section_number":"54.1-3440","catch_line":"Persons to whom nonrestricted permit is granted","url":"\/54.1-3440\/","token":"54.1\/III\/34\/4\/54.1-3440","metadata":false},{"id":368762,"structure_id":52542,"section_number":"54.1-3441","catch_line":"Restricted manufacturing permit; application; fee; separate application and permit for each place of manufacturing","url":"\/54.1-3441\/","token":"54.1\/III\/34\/4\/54.1-3441","metadata":false},{"id":368772,"structure_id":52542,"section_number":"54.1-3442","catch_line":"When permit not to be granted; regulations","url":"\/54.1-3442\/","token":"54.1\/III\/34\/4\/54.1-3442","metadata":false},{"id":368763,"structure_id":52542,"section_number":"54.1-3442.01","catch_line":"Registration of nonresident manufacturer; renewal","url":"\/54.1-3442.01\/","token":"54.1\/III\/34\/4\/54.1-3442.01","metadata":false},{"id":368764,"structure_id":52542,"section_number":"54.1-3442.02","catch_line":"Prescription drug price transparency","url":"\/54.1-3442.02\/","token":"54.1\/III\/34\/4\/54.1-3442.02","metadata":false}],"previous_section":{"id":368758,"structure_id":52542,"section_number":"54.1-3437","catch_line":"Permit to manufacture drugs","url":"\/54.1-3437\/","token":"54.1\/III\/34\/4\/54.1-3437","metadata":false},"next_section":{"id":368759,"structure_id":52542,"section_number":"54.1-3438","catch_line":"Manufacturing, etc., of drugs or proprietary medicines, to be supervised by pharmacist","url":"\/54.1-3438\/","token":"54.1\/III\/34\/4\/54.1-3438","metadata":false},"metadata":false,"official_url":"https:\/\/law.lis.virginia.gov\/vacode\/54.1-3437.1\/","history_text":"

This law was first created in 1997. The record of its establishment is cataloged in chapter 218<\/a> of that year\u2019s edition of \u201cActs of Assembly,\u201d the annual state publication listing all changes made to the Code of Virginia in that year. It has been modified 1 time. Those modifications are cataloged by \u201cThe Acts of Assembly,\u201d a state publication, by year and chapter. Those modifications that can be read on the General Assembly\u2019s website will be linked accordingly. That modification is as follows: in 2009, chapters 813<\/a> and 840<\/a>.<\/p>","references":false,"refers_to":false,"permalink":{"id":1470561,"object_type":"law","relational_id":368757,"identifier":"54.1-3437.1","token":"54.1\/III\/34\/4\/54.1-3437.1","url":"\/54.1-3437.1\/","edition_id":2,"permalink":0,"preferred":1},"url":"\/54.1-3437.1\/","token":"54.1\/III\/34\/4\/54.1-3437.1","dublin_core":{"Title":"Limited permit for repackaging drugs","Type":"Text","Format":"text\/html","Identifier":"\u00a7 54.1-3437.1","Relation":"Code of Virginia"},"html":"\n\t\t\t\t\t\t

The Board<\/span> may issue<\/span> a limited manufacturing permit for the purpose of repackaging drugs<\/span>, upon such terms and conditions approved by the Board<\/span>, to the pharmacy directly operated by the Department of Behavioral Health and Developmental Services and which serves clients of the community services<\/span> boards<\/span>.<\/p><\/section>","plain_text":" CODE OF VIRGINIA\n\nLIMITED PERMIT FOR REPACKAGING DRUGS (\u00a7 54.1-3437.1)\n\nThe Board may issue a limited manufacturing permit for the purpose of\nrepackaging drugs, upon such terms and conditions approved by the Board, to the\npharmacy directly operated by the Department of Behavioral Health and\nDevelopmental Services and which serves clients of the community services\nboards.\n\nHISTORY: 1997, c. 218; 2009, cc. 813, 840.","edition":{"id":2,"name":"2026","slug":"2026","date_created":"2026-07-16 18:40:23","date_modified":"2026-08-02 15:14:36","current":1,"order_by":2,"last_import":"2026-08-02 12:37:30"}}