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`FOOD AND DRUG ADMINISTRATION
`·¸¸¹º»¼¹º¹½¾¿º»¹ÀÁ¼ÁÂý»ÃÁ¸¼º
`CENTER FOR DRUG EVALUATION AND RESEARCH
`ÄżÃŽº·¸½º¹½¾¿ºÅƻǾ»ÃÁ¸¼º»¼¹º½ÅÂÅ»½ÄȺ
`APPROVED DRUG PRODUCTS
`»Éɽ¸ÆŹº¹½¾¿ºÉ½¸¹¾Äú
`with
`ÊËÌͺ
`Therapeutic Equivalence Evaluations
`ÃÍÎÏÐÑÎÒÌËÓºÅÔÒËÕÐÖÎ×ÓκÅÕÐÖÒÐÌËØ×Ùº
`
`CONTENTS
`ĸ¼ÃżÃº
`
`PAGE
`ÚÛÜÝÞ
`PREFACE TO TWENTY NINTH EDITION ............................................................. ..iv
`ßàáâãäáåæçåæèáéæêåéëéæìåáíëæëçéîîîîîîîîîîîîïïïîîîîïïîïïïïïïïðñå
`1
`INTRODUCTION ................................................................................................................. ..vi
`òåëéæàçíóäæëçéïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïñð
`1.1
`Content and Exclusion .................................................................................................... ..vi
`òïòå äôõö÷õöåøõùåáúûüýþðôõïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïñð
`1.2
`Therapeutic Equivalence-Related Terms ....................................................................... ..vi
`òïå æ ÷ø ÷ýöðûåáýðñøü÷õû÷à÷üøö÷ùåæ÷þåïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïñð
`1.3
`Statistical Criteria for Bioequivalence ........................................................................... .. viii
`òïå öøöðþöðûøüåäðö÷ðøå ôå
`ðô÷ýðñøü÷õû÷ïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïñððð
`1.4
`Reference Listed Drug ..................................................................................................... ..x
`òï å à÷ ÷÷õû÷å
ðþö÷ùåíý ïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïú
`1.5
`General Policies and Legal Status .................................................................................. ..x
`òïå ÷õ÷øüåßôüðûð÷þåøõùå
÷ øüåöøöýþåïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïú
`1.6
`Practitioner/User Responsibilities ................................................................................... ..xi
`òïå ßøûöðöðôõ÷óþ÷åà÷þ ôõþððüðöð÷þïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïúð
`1.7
`Therapeutic Equivalence Evaluations Codes ............................................................... .. xiii
`òïå æ ÷ø ÷ýöðûåáýðñøü÷õû÷åáñøüýøöðôõþåäôù÷þïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïúððð
`1.8
`Description of Special Situations ................................................................................... ..xx
`òïå í÷þûð öðôõåô å ÷ûðøüåðöýøöðôõþïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïúú
`1.9
`Therapeutic Equivalence Code Change for a Drug Entity ........................................... .. xxii
`òïå æ ÷ø ÷ýöðûåáýðñøü÷õû÷åäôù÷åä øõ ÷å ôåøåíý åáõöðöïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïåúúðð
`1.10 Change of the Therapeutic Equivalence Evaluation for a Single Product ................... .. xxii
`òïòå ä øõ ÷åô åö ÷åæ ÷ø ÷ýöðûåáýðñøü÷õû÷åáñøüýøöðôõå ôåøåðõ ü÷åßôùýûöïïïïïïïïïïïïïïïïïïïïïúúðð
`1.11
`Discontinued Section .................................................................................................. .. xxiii
`òïòòå íðþûôõöðõý÷ùå÷ûöðôõïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïåúúððð
`1.12 Changes to the Orange Book ..................................................................................... .. xxiii
`òïòå ä øõ ÷þåöôåö ÷åçøõ ÷å
`ôôïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïåúúððð
`1.13 Availability of the Edition ............................................................................................. .. xxiii
`òïòå ãñøðüøðüðöåô åö ÷åáùðöðôõïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïåúúððð
`2
`HOW TO USE THE DRUG PRODUCTS LISTS ............................................................ ..2-1
`å ìçèåæçåóáåæìáåíàóåßàçíóäæå
ëæåïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïïòå
`2.1
`Key Sections for Using the Drug Product Lists ................................................... ..2-1
`ïòå ÷å÷ûöðôõþå ôåóþðõ åö ÷åíý åßôùýûöå
ðþöþåîîîîîîîîïîïîîîîîîïïïïïïòå
`2.2
`Drug Product Illustration ............................................................................... ..2-3
`ïå íý åßôùýûöåëüüýþöøöðôõåîîîîîîîîîîîîîîîîîïïîïîîîîîïîîïïå
`2.3
`Therapeutic Equivalence Evaluations Illustration ............................................... ..2-4
`ïå æ ÷ø ÷ýöðûåáýðñøü÷õû÷åáñøüýøöðôõþåëüüýþöøöðôõåîîîîîîîïîïîîîîïïîîî å
`DRUG PRODUCT LISTS
`íàóåßàçíóäæå
ëæå
`Prescription Drug Product List ................................................................................. ..3-1
`ß÷þûð öðôõåíý åßôùýûöå
ðþöåîîîîîîîîîîîîîîîïîîîîîïîîîîîîïïïòå
`OTC Drug Product List .......................................................................................... ..4-1
`çæäåíý åßôùýûöå
ðþöåîîîîîîîîîîîîîîîîîîïîîîîîïîîîîîîî òå
`Drug Products with Approval under Section 505 of the Act Administered
`íý åßôùýûöþåðö åã ôñøüåýõù÷å÷ûöðôõååô åö ÷åãûöåãùðõðþö÷÷ùå
`by the Center for Biologics Evaluation and Research List ....................................... ..5-1
`åö ÷åä÷õö÷å ôå
`ðôüô ðûþåáñøüýøöðôõåøõùåà÷þ÷øû å
ðþöåïïïîîîïîîïîîîîîîïïïòå
`Discontinued Drug Product List ................................................................................ ..6-1
`íðþûôõöðõý÷ùåíý åßôùýûöå
ðþöåïîîîîîîîîîîîîîîîîîïîîïîîîîîîïïïïòå
`Orphan Products Designations and Approvals List
`...................................................... ..7-1
`ç øõåßôùýûöþåí÷þð õøöðôõþåøõùåã ôñøüþå
ðþöåîîîîîïîîîîïîîïîîîîîîïïòå
`Drug Products Which Must Demonstrate in vivo Bioavailability
`íý åßôùýûöþåè ðû åýþöåí÷ôõþöøö÷åðõåñðñôå
`ðôøñøðüøðüðöå
`Only if Product Fails to Achieve Adequate Dissolution .................................................. ..8-1
`çõüåð åßôùýûöåâøðüþåöôåãû ð÷ñ÷åãù÷ýøö÷åíðþþôüýöðôõåîîîîîîîïïîîîîîîîîîïïòå
`APPENDICES
`ãßßáéíëäáå
`A. Product Name Index ................................................................................ ..A-1
`ãïåßôùýûöåéø÷åëõù÷úåîîîïîïïïîîîîîîîîîîïîîîïïîîîîîîîîãòå
`B. Product Name Index Listed by Applicant ...................................................... ..B-1
`
`
`ïåßôùýûöåéø÷åëõù÷úå
ðþö÷ùååã üðûøõöåîîîîîîîïîîïïîîîîîîîîïï
`òå
`C. Uniform Terms ........................................................................................ ..C-1
`äïåóõð ôåæ÷þåîîîîîîîîîîîîîîîîîïîîîïïîîîîïïïîîîïïïäòå
`PATENT AND EXCLUSIVITY INFORMATION ADDENDUM ............................................ ..AD1
`ßãæáéæåãéíåáä
óëëæêåëéâçàãæëçéåãííáéíóåîîîïîîïïîîîîîîïïïïïïïïïïãíòå
`A. Patent and Exclusivity Lists .................................................................... ..ADA1
`ãïåßøö÷õöåøõùåáúûüýþðñðöå
ðþöþåîîîîîîîîîîîïîïïîîïïîîîîîïïîîãíãòå
`B. Patent and Exclusivity Terms .................................................................. ..ADB1
`
`
`ïåßøö÷õöåøõùåáúûüýþðñðöåæ÷þåïïïîîîîîîîîîïîïîîîïïïîîîîîîîãí
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`EDITION -
`29TH
`2009 - APPROVED DRUG PRODUCTS LIST
`‘’“”•–—’—˜™”š”››‘”š”œž˜Ÿ•–”–ž ¡”ž˜– ¢’£”¤—£’
`PRESCRIPTION DRUG PRODUCT LIST
`3 - 107 (of 376)
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`1983
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`1983
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`2000
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`1990
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`

`

`ADA 36 of 179
`29TH EDITION - 2009 - APPROVED DRUG PRODUCTS LIST
`þøþö ö
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ó
`òóôõö÷øùôùúûöüöòýýóöüöþ ú÷øöø ö úø ôöùôö
`PRESCRIPTION AND OTC DRUG PRODUCT PATENT AND EXCLUSIVITY LIST
`
`See report footnote for information regarding report content
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`30, 2011
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