Pharmaceutical dosage forms : Parenteral medications Volume 1: Formulation and Packaging/ edited by Sandeep Nema and John D. Ludwig.
Material type:
- 9781420086539
- 9781420086430
- 615.19 NEP

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KU Central Library | Rack No. : 27 Shelve No. : A-06 | Reference Section (Non-Issuable Books) | 615.19 NEP (Browse shelf(Opens below)) | 1 | Not For Loan | 36010 | ||
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KU Central Library | Rack No. : 63 Shelve No. : A-03 | General Stack (Issuable Books) | 615.19 NEP 2010 (Browse shelf(Opens below)) | C-3 (I) | Available | 51513 | ||
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KU Central Library | Rack No. : 63 Shelve No. : A-03 | General Stack (Issuable Books) | 615.19 NEP 2010 (Browse shelf(Opens below)) | C-4 (I) | Available | 51514 | ||
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KU Central Library | Rack No. : 63 Shelve No. : A-03 | General Stack (Issuable Books) | 615.19 NEP 2010 (Browse shelf(Opens below)) | C-5 (I) | Available | 53838 | ||
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KU Central Library | Rack No. : 27 Shelve No. : B-03 | Reference Section (Non-Issuable Books) | 615.19 NEP 2010 (Browse shelf(Opens below)) | C-2 (NI) | Not For Loan | 51512 |
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Includes bibliographical references and index.
1.Parenteral Dosage Forms: Introduction and Historical Perspectives
2.Parenteral Drug Administration: Routes of Administration and Devices
3.Biopharmaceutics and Immunogenicity of Biotherapeutics
4.Preformulation Research of Parenteral Medication
5.Formulation Development of Small and Large Volume Injection
6.Solubility and Solubilization
7.Formulation of Depot Delivery Systems
8.Biophysical and Biochemical Characterization of Peptide and Protein Drug Product
9.Formulation of Protein- and Peptide-based Parenteral Products
10.Development of Ophthalmic Formulations
11.Glass containers for Parenteral Products
12.Plastic Packaging for Parenteral Drug Delivery
13.Elastomeric Closures for Parenterals
14.Parenteral Product Container-Closure Integrity Testing
This three-volume set of Pharmaceutical Dosage Forms: Parenteral Medications is an authoritative, comprehensive reference work on the formulation and manufacture of parenteral dosage forms, effectively balancing theoretical considerations with the practical aspects of their development. As such, it is recommended for scientists and engineers in the pharmaceutical industry and academia, and will also serve as an excellent reference and training tool for regulatory scientists and quality assurance professionals.
First published in 1984 (as two volumes) and then last revised in 1993 (when it grew to three volumes), this latest revision will address the plethora of changes in the science and considerable advances in the technology associated with these products and routes of administration. The third edition of this book maintains the features that made the last edition so popular but comprises several brand new chapters, revisions to all other chapters, as well as high quality illustrations.
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