Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 016998
Company: PARKE DAVIS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
UTICORT BETAMETHASONE BENZOATE 0.025% CREAM;TOPICAL Discontinued None 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
06/28/1974 ORIG-1 Approval Type 3 - New Dosage Form STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
03/13/1981 SUPPL-9 Labeling

Label is not available on this site.

11/21/1978 SUPPL-7 Labeling

Label is not available on this site.

12/13/1974 SUPPL-4 Labeling

Label is not available on this site.

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