Production / Manufacturing
Handbook of Pharmaceutical Manufacturing Formulations - Vol 4 of 6
Semisolid Products
| Publication Date | April 2007 |
| Publisher | CRC Press |
| Product Type | Book |
| Pages | 288 |
| ISBN Number | 849317495 |
| Product Code | CRC00102 |
|
Summary
This publication :-- Presents the world's largest reference source on pharmaceutical formulations
- Includes readily accessible formulations listed as chemical entities, dosage forms or pharmacological classifications
- Provides instant substantial time and cost-savings in pharmaceutical research and development
- Speeds generic drug formulation regulatory submissions
The fourth volume in the six-volume Handbook of Pharmaceutical Manufacturing Formulations, this book covers semi-solid drugs. It includes formulations of ointments, lotions, gels, and suppositories, from publicly available but widely dispersed information from FDA New Drug Applications (NDA), patent applications, and other sources of generic and proprietary formulations. Each entry begins with a fully validated scaleable manufacturing formula and a summary of manufacturing process. The book provides a detailed discussion on the difficulties encountered in manufacturing semi-solid drugs, the common elements of formulations. The section on regulatory and manufacturing guidance deals with such topics as changes to approved NDAs and aNDAs, post-approval changes to semisolid drugs, SUPAC for non-sterile semisolid dosage form equipment, stability testing of drugs substances and drug products, guidelines on evaluation of stability data in retest periods, skin irritation and sensitization testing of generic transdermal products, and photosafety testing, in addition to providing quick tips on resolving the common problems in formulating semisolid products.
Contents
Regulatory And Manufacturing Guidance
Changes to Approved New Drug Applications or Abbreviated New Drug Applications
Postapproval Changes to Semisolid Drugs
Scale-Up and Postapproval Changes for Nonsterile Semisolid Dosage Forms: Manufacturing Equipment
Stability Testing of Drug Substances and Drug Products
Guidelines for Evaluation of Stability Data in Retest Periods
Skin Irritation and Sensitization Testing of Generic Transdermal Drug Products
Photosafety Testing Guidance on Formulating Semisolid Drugs
Postapproval Changes to Semisolid Drugs
Scale-Up and Postapproval Changes for Nonsterile Semisolid Dosage Forms: Manufacturing Equipment
Stability Testing of Drug Substances and Drug Products
Guidelines for Evaluation of Stability Data in Retest Periods
Skin Irritation and Sensitization Testing of Generic Transdermal Drug Products
Photosafety Testing Guidance on Formulating Semisolid Drugs
Formulations Of Semisolid Drugs
Entries are arranged in alphabetical order of drug entity
Cross-referenced index allows sorting by the dosage form and by pharmacological class
Cross-referenced index allows sorting by the dosage form and by pharmacological class







