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BACTROBAN از شرکت GLAXOSMITHKLINE

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داروی نمایش داده شده مورد تایید FDA می باشد و اطلاعات ثبت آن در زیر قابل مشاهده است

BACTROBAN از شرکت GLAXOSMITHKLINE

New Drug Application (NDA): 050746

Company: GLAXOSMITHKLINE

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BACTROBAN MUPIROCIN CALCIUM EQ 2% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** CREAM;TOPICAL Discontinued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
12/11/1997 ORIG-1 Approval

Type 3 – New Dosage Form

STANDARD

Review

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/nda/97/050746_bactroban_toc.cfm

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
02/19/2020 SUPPL-22 Labeling-Package Insert, Labeling-Container/Carton Labels

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/050746s022lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/050746Orig1s022ltr.pdf

05/08/2017 SUPPL-21 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/050746s021lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2017/050746Orig1s021ltr.pdf

12/14/2015 SUPPL-20 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/050746s020lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2015/050746Orig1s020ltr.pdf

12/16/2015 SUPPL-19 Manufacturing (CMC)

Label is not available on this site.

05/22/2014 SUPPL-18 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/050591s032,050703s015,050746s018lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/50591Orig1s032,50703Orig1s015,50746Orig1s018ltr.pdf

03/19/2015 SUPPL-13 Labeling

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/050746s013lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2015/050746Orig1s013ltr.pdf

11/15/2001 SUPPL-9 Manufacturing (CMC)-Control

Label is not available on this site.

11/09/2001 SUPPL-8 Manufacturing (CMC)-Control

Label is not available on this site.

09/21/2001 SUPPL-7 Manufacturing (CMC)-Control

Label is not available on this site.

12/13/2000 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

07/14/2000 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

10/06/1999 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

05/19/1999 SUPPL-3 Manufacturing (CMC)-Control

Label is not available on this site.

09/04/1998 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

06/10/1998 SUPPL-1 Manufacturing (CMC)-Packaging

Label is not available on this site.

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
02/19/2020 SUPPL-22

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/050746s022lbl.pdf
02/19/2020 SUPPL-22

Labeling-Container/Carton Labels

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/050746s022lbl.pdf
05/08/2017 SUPPL-21

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/050746s021lbl.pdf
12/14/2015 SUPPL-20

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/050746s020lbl.pdf
03/19/2015 SUPPL-13

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/050746s013lbl.pdf
05/22/2014 SUPPL-18

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/050591s032,050703s015,050746s018lbl.pdf
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