C.F.R. » Title 21 » CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES › SUBCHAPTER C—DRUGS: GENERAL › PART 203—PRESCRIPTION DRUG MARKETING › Subpart A—General Provisions

21 C.F.R. § 203.2

Purpose

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The purpose of this part is to implement the Prescription Drug Marketing Act of 1987 and the Prescription Drug Amendments of 1992, except for those sections relating to State licensing of wholesale distributors (see part 205 of this chapter), to protect the public health, and to protect the public against drug diversion by establishing procedures, requirements, and minimum standards for the distribution of prescription drugs and prescription drug samples.

Notes of Decisions
Cited in 2 cases, 2015–2015 · leading case: State Ex Rel. Wilson v. Ortho-McNeil-Janssen Pharm., Inc., 777 S.E.2d 176 (S.C. 2015).
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State Ex Rel. Wilson v. Ortho-McNeil-Janssen Pharm., Inc., 777 S.E.2d 176 (S.C. 2015). · cites it 2× “, 21 C.F.R. § 203.2 (2014) ("The purpose of this part is .”
State v. Ortho-McNeil-Janssen Pharm. (S.C. 2015). “, 21 C.F.R. § 203.2 (2014) ("The purpose of this part is .”
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