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Chapter 10Annex 1Fitness Information Foaminess information to be provided in connection with an application for inclusion in the relevant pharmaceutical list DAC body corporates form is to be completed
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Refer to the official 21 US Code 353 document for reference.
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Who needs 21 us code353?

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Individuals or entities involved in the distribution or dispensing of prescription drugs need to comply with 21 US Code 353.

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21 U.S. Code § 353 outlines the requirements for labeling of drugs and devices.
Manufacturers, packers, and distributors of drugs and devices are required to comply with the regulations outlined in 21 U.S. Code § 353.
To fill out 21 U.S. Code § 353, one must ensure that all drugs and devices are properly labeled with the required information.
The purpose of 21 U.S. Code § 353 is to ensure that drugs and devices are appropriately labeled to provide crucial information to consumers.
Information such as the name and address of the manufacturer, packer, or distributor, as well as the ingredients and directions for use of the drug or device must be reported on 21 U.S. Code § 353.
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