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approves brand name and generic drugs including lebeling and regulatory? ​

Sagot :

Answer:

While brand name drug refers to the name giving by the producing company, generic drug refers to a drug produced after the active ingredient of the brand name drug. Generic drugs will, however, be sold under different brand names, but will contain the same active ingredients as the brand-name drug.

Explanation:

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Answer:

All generic drugs in the United States are approved by the U.S. Food and Drug Administration (FDA). To get approval, a manufacturer must submit an Abbreviated New Drug Application (ANDA) and show that their generic drug is equivalent to the marketed brand name.

Explanation:

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