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Zdrowie i gospodarka · 07/06/2005

FDA Releases Draft Guidance on Bar Code Label Requirements for Human Drug and Biological Products

The Food and Drug Administration (FDA) has published a draft guidance document to address questions about the application of bar code label requirements for certain human drug and biological products, which are required to display a linear bar code identifying the product's National Drug Code (NDC) number.

Source: Federal Register — Food and Drug AdministrationOpen original release →