Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 077523
Company: IVAX SUB TEVA PHARMS
Company: IVAX SUB TEVA PHARMS
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
FLUCONAZOLE | FLUCONAZOLE | 50MG/5ML | FOR SUSPENSION;ORAL | Discontinued | None | No | No |
FLUCONAZOLE | FLUCONAZOLE | 200MG/5ML | FOR SUSPENSION;ORAL | 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 |
---|---|---|---|---|---|---|---|
09/12/2007 | 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 |
---|---|---|---|---|---|
01/23/2012 | SUPPL-5 | Labeling-Package Insert |
Label is not available on this site. |
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01/23/2012 | SUPPL-4 | Labeling-Package Insert |
Label is not available on this site. |
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12/27/2010 | SUPPL-3 | Labeling-Package Insert |
Label is not available on this site. |
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07/23/2008 | SUPPL-2 | Labeling |
Label is not available on this site. |