Pharmaceutical Dosage Forms

Loyd Vernon Allen Jr.

Loyd Vernon Allen Jr.

International Journal of Pharmaceutical Compounding, Edmond, Oklahoma, 73034 United States

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Paul Zanowiak

Paul Zanowiak

Temple University, Health Sciences Center, Philadelphia, Pennsylvania, 19140 United States

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First published: 19 November 2014
Citations: 1

Abstract

The article contains sections titled:

1. Dosage Forms as Drug Delivery Systems
2. Routes of Administration
2.1. Parenteral Administration
2.2. Oral Administration
2.3. Dermal Administration
2.4. Rectal Administration
2.5. Other Routes of Administration
3. Types of Dosage Forms
3.1. Liquid Solution Dosage Forms
3.1.1. Solutions
3.1.2. Extractive Solutions
3.1.3. Parenteral Solutions (Injections)
3.1.4. Inhalations
3.1.5. Ophthalmic and Nasal Solutions (Drops)
3.1.6. Otic Solutions
3.1.7. Liniments
3.1.8. Enemas and Douches
3.1.9. Mouthwashes and Gargles
3.1.10. Collodions
3.1.11. Soaps and Shampoos
3.2. Liquid Dispersions
3.2.1. Emulsions
3.2.2. Suspension
3.2.3. Foams
3.2.4. Sprays
3.3. Semisolid Dosage Forms
3.3.1. Gels, Magmas, and Mucilages
3.3.2. Ointments, Creams, Pastes, and Plasters
3.4. Plastic Dosage Forms
3.4.1. Suppositories
3.4.2. Inserts
3.4.3. Implants
3.4.4. Pellets
3.5. Solid Dosage Forms
3.5.1. Bulk Powders and Effervescent Powders
3.5.2. Dusting Powders
3.5.3. Insufflations
3.5.4. Lyophilized Powders
3.5.5. Capsules
3.5.6. Cachets
3.5.7. Pills
3.5.8. Tablet Triturates, Hypodermic Tablets
3.5.9. Troches and Lozenges
3.5.10. Gums
3.5.11. Films
3.5.12. Strips
3.5.13. Tapes
3.5.14. Granules
3.5.15. Compressed Tablets
3.6. Prolonged-Action Dosage Forms
3.7. Pressurized Aerosol Dosage Forms
3.8. Nonpressurized Gaseous Dosage Forms (Inhalants)
3.9. Radiopharmaceutical Dosage Forms
4. Active Pharmaceutical Ingredients (APIs)
4.1. Hydrates and Solvates
4.2. Organic Salts
4.3. Esters
4.4. Inorganic Salts
4.5. Potency-Designated Ingredients
4.6. Complex Organic Molecules
4.7. Aliquots, Dilutions, and Concentrates
4.8. Product Quality Tests
5. Pharmaceutical Excipients
5.1. Formulation Excipients
5.2. Patient Compliance Excipients
5.3. Stability Excipients
6. Quality Assurance
7. Pharmaceutical Containers
8. Development of the Ideal Drug Delivery System
8.1. Controlled-Release Drug Delivery Systems
8.2. Sustained- or Prolonged-Release Technology
8.2.1. Oral Sustained-Release Dosage Forms
8.2.2. Other Sustained- and Prolonged-Release Drug Delivery Systems
8.3. Targeted Drug Delivery Systems

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