64B16-27.510. Identification of Manufacturer

Effective on Thursday, October 8, 2015

1Each formulary of generic and brand name drug products established by each community pharmacy pursuant to the provisions of Section 21465.025, F.S., 23shall include the name of the manufacturer of the generic drug listed in said formulary.

38Rulemaking Authority 40465.005 FS. 42Law Implemented 44465.025 FS. 46History–New 3-16-77, Formerly 21S-5.02, 21S-5.002, 21S-27.510, 61F10-27.510, 59X-27.510.

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16367021. The Board proposes to repeal the rules due to ...

                    
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