Application 018922

Type
NDA
Sponsor
WYETH PHARMS INC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
002LODINEETODOLACCAPSULE;ORAL200MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
003LODINEETODOLACCAPSULE;ORAL300MGYesNo
004LODINEETODOLACTABLET;ORAL400MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo
005LODINEETODOLACTABLET;ORAL500MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**YesNo

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
57655SUPPL2019-02-15
33648SUPPL2015-07-27
16096SUPPL2007-10-15
33647SUPPL2006-01-20
16095SUPPL2006-01-20
16094SUPPL2005-05-27
11362SUPPL2005-05-27