Subjects: Prescription Drugs and Government Regulation - Digital Collections - National Library of Medicine Search Results

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1. Instructions for use: patient labeling for human prescription drug and biological products : content and format

Publication:: Silver Spring, MD : Center for Drug Evaluation and Research, July 2022
Subject(s):: Biological Products
Government Regulation
Prescription Drugs
Product Labeling
United States
United States. Food and Drug Administration

2. Part D plans generally include drugs commonly used by dual eligibles: 2022

Publication:: Washington, D.C. : U.S. Department of Health and Human Services, Office of Inspector General, June 2022
Subject(s):: Dual MEDICAID MEDICARE Eligibility
Government Regulation
Medicare Part D
Prescription Drugs
United States

3. Part D plans generally include drugs commonly used by dual-eligible enrollees: 2023

Publication:: Washington, D.C. : U.S. Department of Health and Human Services, Office of Inspector General, July 2023
Subject(s):: Dual MEDICAID MEDICARE Eligibility
Formularies as Topic
Government Regulation
Medicare Part D
Prescription Drugs
United States

4. Direct-to-consumer prescription drug advertisements: presentation of the major statement in a clear, conspicuous, and neutral manner in advertisements in television and radio format final rule : questions and answers : guidance for industry

Publication:: Silver Spring, MD : Center for Drug Evaluation and Research, December 2023
Subject(s):: Direct-to-Consumer Advertising -- legislation & jurisprudence
Drug Industry
Government Regulation
Legislation, Drug
Prescription Drugs
United States