Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 076603
Company: ANDA REPOSITORY
Company: ANDA REPOSITORY
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
BETAMETHASONE DIPROPIONATE | BETAMETHASONE DIPROPIONATE | EQ 0.05% BASE | CREAM, 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 |
---|---|---|---|---|---|---|---|
01/23/2004 | 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 |
---|---|---|---|---|---|
06/04/2015 | SUPPL-17 | Labeling-Package Insert |
Label is not available on this site. |
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11/28/2012 | SUPPL-16 | Labeling-Package Insert, Labeling-Container/Carton Labels |
Label is not available on this site. |
||
07/21/2009 | SUPPL-11 | Labeling |
Label is not available on this site. |
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05/26/2009 | SUPPL-10 | Labeling |
Label is not available on this site. |