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EPA/WATER RIN: 2040-AA13 Publication ID: Fall 1995 
Title: Effluent Guidelines and Standards for the Pharmaceutical Manufacturing Category 
Abstract: The Agency will review and revise as appropriate the effluent limitation guidelines and standards for the pharmaceutical manufacturing industry. A major part of the review will consider the inclusion of limitations on toxic and non-conventional volatile organic pollutants. The 1983 proposal covering New Source Performance Standards (NSPS) for conventional pollutants will also be reevaluated. 
Agency: Environmental Protection Agency(EPA)  Priority: Other Significant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Final Rule Stage 
CFR Citation: 40 CFR 439   
Legal Authority: 33 USC 1311/CWA 301    33 USC 1314/CWA 304    33 USC 1316/CWA 306    33 USC 1317/CWA 307    33 USC 1361/CWA 501   
Legal Deadline:
Action Source Description Date
NPRM  Judicial    02/28/1995 
Final  Judicial  Dates contained in Consent Decree (NRDC v. Reilly).  08/31/1996 
Timetable:
Action Date FR Cite
NPRM (NSPS)  10/27/1983  48 FR 49832   
NPRM  05/02/1995  60 FR 21592   
Final Action  08/00/1996    
Additional Information: SAN No. 1427. ^PRFA: Y
Regulatory Flexibility Analysis Required: No  Government Levels Affected: Federal, Local, State 
Included in the Regulatory Plan: No 
Agency Contact:
Frank Hund
Environmental Protection Agency
Water
4303,
Washington, DC 20460
Phone:202 260-7182
Fax:202 260-7185
Email: hund.frank@epa.gov