Drugs@FDA: FDA Approved Drug Products

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New Drug Application (NDA): 019408
Company: SCHERING
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
DIPROLENE BETAMETHASONE DIPROPIONATE EQ 0.05% BASE CREAM, AUGMENTED;TOPICAL Discontinued None No No
DIPROLENE BETAMETHASONE DIPROPIONATE EQ 0.05% BASE GEL, AUGMENTED;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
01/31/1986 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
12/07/2007 SUPPL-15 Labeling

Label is not available on this site.

05/14/1999 SUPPL-14 Manufacturing (CMC)-Control

Label is not available on this site.

11/10/1998 SUPPL-13 Manufacturing (CMC)-Packaging

Label is not available on this site.

06/15/1998 SUPPL-12 Manufacturing (CMC)-Control

Label is not available on this site.

07/31/1998 SUPPL-11 Manufacturing (CMC)-Control

Label is not available on this site.

06/15/1998 SUPPL-10 Manufacturing (CMC)-Control

Label is not available on this site.

12/07/2007 SUPPL-9 Labeling

Label is not available on this site.

11/30/1995 SUPPL-8 Manufacturing (CMC)-Control

Label is not available on this site.

12/08/1993 SUPPL-7 Manufacturing (CMC)-Control

Label is not available on this site.

11/22/1991 SUPPL-6 Manufacturing (CMC)-Formulation

Label is not available on this site.

08/01/1990 SUPPL-5 Manufacturing (CMC)-Control

Label is not available on this site.

05/24/1989 SUPPL-4 Labeling

Label is not available on this site.

12/07/2007 SUPPL-3 Labeling

Label is not available on this site.

02/24/1987 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

05/13/1986 SUPPL-1 Manufacturing (CMC)-Control

Label is not available on this site.

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