International Journal Of Drug Regulatory Affairs

  • Year: 2021
  • Volume: 9
  • Issue: 3

The Purple Book: Evaluations, Approvals and recent updates

  • Author:
  • K Raja Rajeswari1, G Subba Ram Prasad2, Jyothsna B Naga3, Krishna C Murali4, Sekhar P Raja1, V Rama Mohan Gupta1
  • Total Page Count: 5
  • Page Number: 32 to 36

1Pulla Reddy Institute of Pharmacy, Dundigul, Sangareddy Dist., Telangana, India-50231322

2Regulatory Affairs, APL Research Centre, Aurobindo Pharma Ltd, Bachupally, RR Dist, Hyderabad, Telangana, India-500 090

3Malla Reddy Pharmacy College, Dhulapally, Secunderabad, Telangana, India-500 100

4Shadan College of Pharmacy, Peerancheru, Hyderabad, Telangana, 500 091

*Corresponding author

Online Published on 16 December, 2021.

Abstract

The Purple Book is an informative database of all FDA-licensed biological products regulated by the Center for Drug Evaluation and Research (CDER), including licensed biosimilar and interchangeable products, and their reference products. and allergenic, cellular and gene therapy, hematologic, and vaccine products regulated by the Center for Biologics Evaluation and Research (CBER). The current article emphasizes the significance of the Purple Book and the new law, The Purple Book Continuing Act enacted about approved patented biologic products, marketing status etc. The Act codifies a number of FDA's current Purple Book practices, and imposes a new requirement for publishing the reference product sponsor's "patent lists" exchanged in the so-called "patent dance" of BPCIA biosimilar litigation. Biologics approved for 2020–21 are listed.

Keywords

CDER, USFDA, BPCIA, Biological products, Purple Book, FDA, CBER, Biosimilar product