FDA ORANGE BOOK
(Approved
Drug Products with Therapeutic Equivalence Evaluations)
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“The Orange Book" is actually the U.S. Food and Drug Administration's (FDA) official listing of Approved Drug Products with Therapeutic Equivalences.
“Orange book” is published by the FDA's Centre
for Drug Evaluation and Research (CDER).The List contains therapeutic
equivalence evaluations for approved multisource prescription drug products. Generic drug evaluations contained in the
list are designed to serve as public education and advice to physicians, pharmacists
and state health agencies, and to help promote access to lower priced
medicines.
The Orange Book
is divided into four parts: Part one includes approved prescription drug
products with therapeutic equivalence evaluations. Part two lists approved
over-the-counter (OTC) drug products for those drugs that may not be marketed
without NDAs or ANDAs because they are not covered under existing OTC
monographs. Part three includes drug products administered by the Center for
Biologics Evaluation and Research. Part four includes a list of approved
products that have never been marketed, are for export only, are intended for
military use, have been discontinued from marketing, or have had their
approvals withdrawn for reasons other than safety or efficacy.
The therapeutic
equivalence evaluations contained in the list refer to the FDA's criteria for
approved multi-source prescription drug products. The evaluations are presented
in code letters corresponding to the type of evaluation used. An explanation of
the code appears in the introduction to the list. The main criteria for the
inclusion of a drug product on the list are that the product has received an
effective approval that has not been withdrawn for efficacy or safety or
efficacy causes. Inclusion of products on the list is independent of any
current regulatory action through administrative or judicial means against a
drug product.
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