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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 070281
Company: ACTAVIS MID ATLANTIC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE EQ 0.05% BASE LOTION;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
07/31/1985 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
01/22/2003 SUPPL-20 Labeling

Label is not available on this site.

07/19/1995 SUPPL-18 Labeling

Label is not available on this site.

12/23/1994 SUPPL-17 Manufacturing (CMC)

Label is not available on this site.

07/15/1992 SUPPL-16 Manufacturing (CMC)

Label is not available on this site.

04/06/1992 SUPPL-15 Manufacturing (CMC)

Label is not available on this site.

03/05/1991 SUPPL-14 Labeling

Label is not available on this site.

04/20/1992 SUPPL-13 Manufacturing (CMC)

Label is not available on this site.

09/28/1990 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

10/09/1990 SUPPL-10 Labeling

Label is not available on this site.

01/23/1991 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

02/15/1989 SUPPL-8 Manufacturing (CMC)

Label is not available on this site.

02/15/1989 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

02/15/1989 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

11/06/1987 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

10/09/1986 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

07/21/1986 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

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