Record Display for the EPA National Library Catalog


Main Title Proposed development document for new source performance standards for the pharmaceutical manufacturing point source category.
CORP Author Environmental Protection Agency, Washington, DC. Effluent Guidelines Div.
Publisher Effluent Guidelines Division, Office of Water, U.S. Environmental Protection Agency,
Year Published 1982
Report Number EPA/440/1-82/084B
Stock Number PB93-208221
Subjects Effluent quality--United States ; Drug factories--Environmental aspects--United States ; Water pollution control industry--United States
Additional Subjects Drug industry ; Industrial waste treatment ; Chemical effluents ; Pollution regulations ; Water pollution control ; Water pollution abatement ; Waste water ; Point sources ; Industrial plants ; Water pollution sampling ; Water pollution economics ; Economic impact ; Pretreatment ; Treatment technology ; BAT(Best available technology)
Library Call Number Additional Info Location Last
NTIS  PB93-208221 Some EPA libraries have a fiche copy filed under the call number shown. 07/26/2022
Collation 513 pages ; 28 cm
The document presents the technical data to support effluent limitations for the pharmaceutical manufacturing point source category as required by the Clean Water Act (The Act) and related settlement agreements. It also presents the technologies to achieve limitations as defined by an amended best practicable control technology currently available (BPT), best available technology economically achievable (BAT) and best conventional pollutant control technology (BCT), and standards as defined by new source performance standards (NSPS), and pretreatment standards for new and existing sources (PSNS and PSES). The pharmaceutical manufacturing point source category manufactureres biological products, medicinal chemicals, botanical products and pharmaceutical products covered by Standard Industrial Classification Code (SIC) Numbers 2831, 2833, and 2834, and other commodities described within the report.
Cover title: Development document for effluent limitations guidelines and standards for the pharmaceuticals manufacturing. "November 1982." "EPA 440/1-82/084-b"--Cover. Includes bibliographical references. Microfiche.