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Development Document for Effluent Limitations Guidelines and Standards for the Pharmaceutical Manufacturing Point Source Category [Final]

EPA Number: 440183084
Date of Publication:September, 1983
Pages:274
Audienceindustry

Available from:
WEBhttp://nepis.epa.gov/Exe/ZyPURL.cgi?Dockey=000014OZ.txt
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NTIS# PB84-180066Ordering Information
This document presents the findings of a study of the Pharmaceutical Manufacturing Point Source Category for the purpose of finalizing effluent limitations guidelines for existing and new point sources and to establish pretreatment standards for existing and new dischargers to publicly owned treatment works to implement Sections 301, 303, 306, 307, 308 and 501 of the Clean Water Act. More...

Keywords:
Water Pollution Control
Drug Industry
Industrial Waste Treatment
Cost Analysis
Pretreatment (water)
Water Pollution Abatement
New Source Performance Standards
Best Available Technology (BAT)
Pharmaceutical Manufacturing
Point Source Category
Pharmaceuticals


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