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

21 CFR 330.3: Imprinting of solid oral dosage form drug products.

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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 330—OVER-THE-COUNTER (OTC) HUMAN DRUGS WHICH ARE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED
  5. Subpart A—General Provisions

A requirement to imprint an identification code on solid oral dosage form drug products is set forth under part 206 of this chapter.

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

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