اطلاعات داروی نمایش داده شده مستقیما از دیتابیس اطلاعات دارویی سازمان غذا و دارو آمریکا (FDA) استخراج می شود و مرتبا به روز رسانی می شود
داروی نمایش داده شده مورد تایید FDA می باشد و اطلاعات ثبت آن در زیر قابل مشاهده است
ACLOVATE از شرکت FOUGERA PHARMS
New Drug Application (NDA): 018707
Company: FOUGERA PHARMS
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
ACLOVATE | ALCLOMETASONE DIPROPIONATE | 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | CREAM;TOPICAL | Discontinued |
None |
Yes | 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 |
---|---|---|---|---|---|---|---|
12/14/1982 | 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 |
---|---|---|---|---|---|
04/05/2011 | SUPPL-12 | Labeling |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/018707s012lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2011/018707s012,018702s011ltr.pdf |
||
06/03/2002 | SUPPL-9 | Manufacturing (CMC) |
Label is not available on this site. |
||
04/02/2003 | SUPPL-8 | Labeling |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2003/018707s008lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2003/18707slr008,18702slr007ltr.pdf |
||
04/26/1996 | SUPPL-7 | Efficacy-New Patient Population |
Label is not available on this site. |
||
06/22/1994 | SUPPL-6 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
06/07/1994 | SUPPL-4 | Manufacturing (CMC) |
Label is not available on this site. |
||
02/08/1990 | SUPPL-3 | Manufacturing (CMC) |
Label is not available on this site. |
||
05/20/1986 | SUPPL-2 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
11/03/1983 | SUPPL-1 | Labeling |
Label is not available on this site. |
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
---|---|---|---|---|---|
04/05/2011 | SUPPL-12 |
Labeling |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/018707s012lbl.pdf | |
04/02/2003 | SUPPL-8 |
Labeling |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2003/018707s008lbl.pdf |
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