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EPA - 40 CFR PART 439

PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY

active, Most Current
Organization: EPA
Publication Date: 1 July 2014
Status: active
Page Count: 13
scope:

Applicability.

(a) This part applies to process wastewater discharges resulting from the research and manufacture of pharmaceutical products, which are generally, but not exclusively, reported under SIC 2833, SIC 2834 and SIC 2836 (1987 Standard Industrial Classification Manual).

(b) Although not reported under SIC 2833, SIC 2834 and SIC 2836, discharges from the manufacture of other pharmaceutical products to which this part applies include (but are not limited to):

(1) Products manufactured by one or more of the four types of manufacturing processes described in subcategories A, B, C or D of this part, and considered by the Food and Drug Administration to be pharmaceutical active ingredients;

(2) Multiple end-use products (e.g., components of formulations, chemical intermediates, or final products) derived from pharmaceutical manufacturing operations and intended for use primarily in pharmaceutical applications;

(3) Pharmaceutical products and intermediates not subject to other categorical limitations and standards, provided the manufacturing processes generate process wastewaters that are similar to those derived from the manufacture of pharmaceutical products elsewhere (an example of such a product is citric acid);

(4) Cosmetic preparations that are reported under SIC 2844 and contain pharmaceutical active ingredients, or active ingredients that are intended for the treatment of a skin condition. (These preparations do not include products such as lipsticks or perfumes that serve to enhance appearance, or provide a pleasing odor, but do not enhance skin care. Also excluded are deodorants, manicure preparations, shaving preparations and non-medicated shampoos that do not function primarily as a skin treatment.)

(c) The provisions of this part do not apply to wastewater discharges resulting from the manufacture of the following products,

Document History

July 1, 2022
PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
A description is not available for this item.
July 1, 2021
PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
A description is not available for this item.
July 1, 2020
PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
A description is not available for this item.
July 1, 2018
PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
A description is not available for this item.
July 1, 2017
PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
Applicability. (a) This part applies to process wastewater discharges resulting from the research and manufacture of pharmaceutical products, which are generally, but not exclusively, reported under...
July 1, 2016
PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
Applicability. (a) This part applies to process wastewater discharges resulting from the research and manufacture of pharmaceutical products, which are generally, but not exclusively, reported under...
July 1, 2015
PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
Applicability. (a) This part applies to process wastewater discharges resulting from the research and manufacture of pharmaceutical products, which are generally, but not exclusively, reported under...
40 CFR PART 439
July 1, 2014
PHARMACEUTICAL MANUFACTURING POINT SOURCE CATEGORY
Applicability. (a) This part applies to process wastewater discharges resulting from the research and manufacture of pharmaceutical products, which are generally, but not exclusively, reported under...
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