Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 090727
Company: AKORN
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
DESOXIMETASONE DESOXIMETASONE 0.05% GEL;TOPICAL Prescription AB No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
03/10/2011 ORIG-1 Approval

Label is not available on this site.

DESOXIMETASONE

GEL;TOPICAL; 0.05%
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
DESOXIMETASONE DESOXIMETASONE 0.05% GEL;TOPICAL Prescription No AB 090727 AKORN
DESOXIMETASONE DESOXIMETASONE 0.05% GEL;TOPICAL Prescription No AB 204675 ANDA REPOSITORY
DESOXIMETASONE DESOXIMETASONE 0.05% GEL;TOPICAL Prescription No AB 077552 PERRIGO NEW YORK
TOPICORT DESOXIMETASONE 0.05% GEL;TOPICAL Prescription No AB 074904 TARO PHARM INDS LTD

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