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Compounded Nonsterile Preparations and FDA-Approved Commercially Available Liquid Products for Children: A North American Update
| Content Provider | MDPI |
|---|---|
| Author | Raimar, Löbenberg Parrish, Richard H. Ashworth, Lisa D. Benavides, Sandra Cies, Jeffrey J. Arthur, Robert B. Mac |
| Copyright Year | 2022 |
| Description | The purpose of this work was to evaluate the suitability of recent US Food and Drug Administration (US-FDA)-approved and marketed oral liquid, powder, or granule products for children in North America, to identify the next group of Active Pharmaceutical Ingredients (APIs) that have high potential for development as commercially available FDA-approved finished liquid dosage forms, and to propose lists of compounded nonsterile preparations (CNSPs) that should be developed as commercially available FDA-approved finished liquid dosage forms, as well as those that pharmacists should continue to compound extemporaneously. Through this identification and categorization process, the pharmaceutical industry, government, and professionals are encouraged to continue to work together to improve the likelihood that patients will receive high-quality standardized extemporaneously compounded CNSPs and US-FDA-approved products. |
| Starting Page | 1032 |
| e-ISSN | 19994923 |
| DOI | 10.3390/pharmaceutics14051032 |
| Journal | Pharmaceutics |
| Issue Number | 5 |
| Volume Number | 14 |
| Language | English |
| Publisher | MDPI |
| Publisher Date | 2022-05-10 |
| Access Restriction | Open |
| Subject Keyword | Pharmaceutics Active Pharmaceutical Ingredient Compounded Drug Compounding Extemporaneous Formulation Manufactured Material Medication Monograph Pediatric Reference Standards |
| Content Type | Text |
| Resource Type | Article |
