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EPA/WATER RIN: 2040-AA13 Publication ID: Fall 1997 
Title: Effluent Guidelines and Standards for the Pharmaceutical Manufacturing Category 
Abstract: EPA is developing revised effluent limitation guidelines and standards for the pharmaceutical manufacturing industry, including limitations on toxic and non-conventional volatile organic pollutants. EPA intends to promulgate this rule concurrently with air emission standards. See separate entry for "NESHAP: Pharmaceuticals Production" (RIN 2060-AE83). 
Agency: Environmental Protection Agency(EPA)  Priority: Other Significant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Final Rule Stage 
Major: No  Unfunded Mandates: No 
CFR Citation: 40 CFR 439   
Legal Authority: 33 USC 1311    Clean Water Act sec 301    33 USC 1314    Clean Water Act sec 304    33 USC 1316    Clean Water Act sec 306    33 USC 1317    Clean Water Act sec 307    33 USC 1361    Clean Water Act sec 501   
Legal Deadline:
Action Source Description Date
Final  Judicial    04/30/1998 
NPRM  Judicial    02/28/1995 
Timetable:
Action Date FR Cite
NPRM (NSPS)  10/27/1983  48 FR 49832   
NPRM  05/02/1995  60 FR 21592   
Final  04/00/1998    
Additional Information: SAN No. 1427. ^PRFA: N
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