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HHS/FDA | RIN: 0910-AA49 | Publication ID: Fall 1998 |
Title: Registration of Producers of Drugs and Listing of Drugs in Commercial Distribution | |
Abstract: The proposed rule would revise the regulations under part 207 to clarify the burden on manufacturers, packers, and distributors and to consolidate, reorganize, and streamline the requirements. | |
Agency: Department of Health and Human Services(HHS) | Priority: Other Significant |
RIN Status: Previously published in the Unified Agenda | Agenda Stage of Rulemaking: Long-Term Actions |
Major: Undetermined | Unfunded Mandates: Undetermined |
CFR Citation: 21 CFR 207 | |
Legal Authority: 21 USC 331 21 USC 351 21 USC 352 21 USC 355 21 USC 356 21 USC 357 21 USC 360 21 USC 371 |
Timetable:
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Regulatory Flexibility Analysis Required: Undetermined | Government Levels Affected: Undetermined |
Included in the Regulatory Plan: No | |
Agency Contact: Lee D. Korb Regulatory Counsel Department of Health and Human Services Food and Drug Administration Suite 3037 (HFD-7), Center for Veterinary Medicine, 7519 Standish Place, Room 164, MPN-4, HFV-200, Rockville, MD 20855 Phone:240 276-9258 Fax:240 276-7692 Email: lee.korb@fda.hhs.gov |