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Form Approved: OMB No. 09100025 Expiration Date: August 31, 2023FORM FDA 3626 ×10×20× A Guide for the Submission of Initial Reports on Diagnostic Ray Systems and Their Major ComponentsPublic reporting
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Form FDA 3626 1020 is a form used to report on certain drug products.
Manufacturers, distributors, and importers of drug products are required to file form FDA 3626 1020.
Form FDA 3626 1020 can be filled out electronically through the FDA's online portal or submitted via mail.
The purpose of form FDA 3626 1020 is to provide the FDA with information about drug products in the market.
Information such as product name, dosage form, packaging type, and marketing status must be reported on form FDA 3626 1020.
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