Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 017818
Company: WESTWOOD SQUIBB
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
HALOG HALCINONIDE 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
06/15/1977 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
11/26/1982 SUPPL-9 Labeling

Label is not available on this site.

03/24/1980 SUPPL-8 Labeling

Label is not available on this site.

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