{"formats":[{"name":"JSON","format":"json","url":"\/downloads\/2026\/code-json\/54.1-3439.json"},{"name":"Plain Text","format":"text","url":"\/downloads\/2026\/code-text\/54.1-3439.txt"},{"name":"XML","format":"xml","url":"\/downloads\/2026\/code-xml\/54.1-3439.xml"},{"name":"HTML","format":"html","url":"\/downloads\/2026\/code-html\/54.1-3439.html"}],"law_id":368760,"edition_id":2,"section_id":368760,"structure_id":52542,"section_number":"54.1-3439","catch_line":"Application for nonrestricted manufacturing permit; fee","history":"1970, c. 650, \u00a7 54-524.40; 1972, c. 798; 1976, c. 614; 1980, c. 288; 1988, c. 765; 1996, cc. 37, 407; 2008, c. 320.","full_text":"Every person desiring to manufacture any drug or proprietary medicines shall annually apply to the Board for a nonrestricted manufacturing permit. The application shall be accompanied by the required fee. Separate applications shall be made and separate permits issued for each specific place of manufacturing. Each such permit shall expire annually on a date determined by the Board in regulation.\n\n","order_by":null,"text":{"0":{"id":1374295,"text":"Every person desiring to manufacture any drug or proprietary medicines shall annually apply to the Board for a nonrestricted manufacturing permit. The application shall be accompanied by the required fee. Separate applications shall be made and separate permits issued for each specific place of manufacturing. Each such permit shall expire annually on a date determined by the Board in regulation.","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":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},"next_section":{"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},"metadata":false,"official_url":"https:\/\/law.lis.virginia.gov\/vacode\/54.1-3439\/","history_text":"<p>This law was first created in 1970. The record of its establishment is cataloged in chapter 650 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. Unfortunately, the 1970 \u201cActs\u201d aren\u2019t available online. It has been modified 6 times. 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. Those modifications are as follows: in 1972, chapter 798; in 1976, chapter 614; in 1980, chapter 288; in 1988, chapter 765; in 1996, chapters <a href=\"https:\/\/legacylis.virginia.gov\/cgi-bin\/legp604.exe?961+ful+CHAP0037\">37<\/a> and <a href=\"https:\/\/legacylis.virginia.gov\/cgi-bin\/legp604.exe?961+ful+CHAP0407\">407<\/a>; in 2008, chapter <a href=\"https:\/\/legacylis.virginia.gov\/cgi-bin\/legp604.exe?081+ful+CHAP0320\">320<\/a>.<\/p>","references":false,"refers_to":false,"permalink":{"id":1470569,"object_type":"law","relational_id":368760,"identifier":"54.1-3439","token":"54.1\/III\/34\/4\/54.1-3439","url":"\/54.1-3439\/","edition_id":2,"permalink":0,"preferred":1},"url":"\/54.1-3439\/","token":"54.1\/III\/34\/4\/54.1-3439","dublin_core":{"Title":"Application for nonrestricted manufacturing permit; fee","Type":"Text","Format":"text\/html","Identifier":"\u00a7 54.1-3439","Relation":"Code of Virginia"},"html":"\n\t\t\t\t\t\t<section><p>Every <span class=\"dictionary\">person<\/span> desiring to <span class=\"dictionary\">manufacture<\/span> any <span class=\"dictionary\">drug<\/span> or <span class=\"dictionary\">proprietary medicines<\/span> shall annually apply to the <span class=\"dictionary\">Board<\/span> for a nonrestricted manufacturing permit. The application shall be accompanied by the required fee. Separate applications shall be made and separate permits issued for each specific place of manufacturing. Each such permit shall expire annually on a date determined by the <span class=\"dictionary\">Board<\/span> in regulation.<\/p><\/section>","plain_text":"                                 CODE OF VIRGINIA\n\nAPPLICATION FOR NONRESTRICTED MANUFACTURING PERMIT; FEE (\u00a7 54.1-3439)\n\nEvery person desiring to manufacture any drug or proprietary medicines shall\nannually apply to the Board for a nonrestricted manufacturing permit. The\napplication shall be accompanied by the required fee. Separate applications\nshall be made and separate permits issued for each specific place of\nmanufacturing. Each such permit shall expire annually on a date determined by\nthe Board in regulation.\n\nHISTORY: 1970, c. 650, \u00a7 54-524.40; 1972, c. 798; 1976, c. 614; 1980, c. 288;\n1988, c. 765; 1996, cc. 37, 407; 2008, c. 320.","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"}}