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Federal regulations · Through 2026-08-25 · Newer source version available

21 CFR 314.152: Notice of withdrawal of approval of an application or abbreviated application for a new drug.

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Where this section sits in the code
  1. Title 21—Food and Drugs
  2. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  3. SUBCHAPTER D—DRUGS FOR HUMAN USE
  4. PART 314—APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG
  5. Subpart D—FDA Action on Applications and Abbreviated Applications

If the Food and Drug Administration withdraws approval of an application or abbreviated application for a new drug, FDA will publish a notice in the Federal Register announcing the withdrawal of approval. If the application or abbreviated application was withdrawn for grounds described in § 314.150(a) or § 314.151, the notice will announce the removal of the drug from the list of approved drugs published under section 505(j)(6) of the act and shall satisfy the requirement of § 314.162(b).

Collected 2026-08-27T02:24:47Z. Source file · JSON

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