Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 077236
Company: FOUGERA PHARMS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
PREDNICARBATE PREDNICARBATE 0.1% OINTMENT;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
03/09/2007 ORIG-1 Approval Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2007/077236s000ltr.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
09/25/2015 SUPPL-1 Labeling-Package Insert

Label is not available on this site.

PREDNICARBATE

OINTMENT;TOPICAL; 0.1%
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
DERMATOP PREDNICARBATE 0.1% OINTMENT;TOPICAL Prescription Yes AB 019568 VALEANT PHARMS NORTH
PREDNICARBATE PREDNICARBATE 0.1% OINTMENT;TOPICAL Prescription No AB 077236 FOUGERA PHARMS

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