Transcription of 659 PACKAGING AND STORAGE REQUIREMENTS
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Printed on: Fri Jan 17 2020, 12:08:20 pmCurrently Official as of: 17-Jan-2020 Official as of 1-May-2017 DocId: GUID-48C0134E-8117-4B3B-8DC4-EA70C93 EEE8F_3_en-USPrinted from: 2020 USPC 659 PACKAGING AND STORAGE REQUIREMENTS (A portion of theAssociated Componentssection of this chapter will become official on May 1, 2019, and a portion of the Packagingsection of this chapter will become official on May 1, 2020, as indicated. Early adoption of the REQUIREMENTS in this chapter and Plastic Materials of Construction and Plastic PACKAGING Systems for Pharmaceutical Use are permitted by USP.)INTRODUCTIONThe purpose of this chapter is to provide PACKAGING definitions, auxiliary PACKAGING information, and STORAGE condition definitions relevant to the STORAGE and distribution of active ingredients, excipients, and medical products, such as pharmaceuticals, devices, combination products ( , drug-eluting stents), and dietary supplements.
packaging [Child-resistant and Senior-friendly packaging(16 CFR §1700.15 et seq.)]. For oral medicinal liquids, surface and flow characteristics vary. It is the responsibility of the manufacturer to ensure that all components of the Restricted delivery system provide the intended safety protection. One component of the
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