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BINOSTO از شرکت ASCEND THERAPS US

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BINOSTO از شرکت ASCEND THERAPS US

New Drug Application (NDA): 202344

Company: ASCEND THERAPS US

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BINOSTO ALENDRONATE SODIUM EQ 70MG BASE TABLET, EFFERVESCENT;ORAL Prescription

None

Yes Yes
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
03/12/2012 ORIG-1 Approval

Type 3 – New Dosage Form

STANDARD

Label (PDF)

Letter (PDF)

Review

Summary Review (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/202344s000lbl.pdf
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/202344s000ltr.pdf
https://www.accessdata.fda.gov/drugsatfda_docs/nda/2012/202344_binosto_toc.cfm
https://www.accessdata.fda.gov/drugsatfda_docs/nda/2012/202344Orig1s000SumR.pdf

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
10/13/2020 SUPPL-15 Labeling

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/202344s015lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/202344Orig1s015ltr.pdf

06/08/2020 SUPPL-13 Labeling-Medication Guide, Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/202344s013lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/202344Orig1s013ltr.pdf

12/30/2016 SUPPL-11 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/202344s011lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/202344Orig1s011ltr.pdf

03/22/2016 SUPPL-10 Labeling-Container/Carton Labels

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/202344Orig1s010ltr.pdf

01/26/2016 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

04/08/2015 SUPPL-8 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/202344s008lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2015/202344Orig1s008ltr.pdf

02/26/2015 SUPPL-7 Labeling-Container/Carton Labels

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/202344s007lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2015/202344Orig1s007ltr.pdf

12/23/2013 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

04/17/2013 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

08/02/2013 SUPPL-2 Manufacturing (CMC)

Label (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/202344s002lbl.pdf

04/19/2013 SUPPL-1 Labeling-Container/Carton Labels, Labeling-Medication Guide, Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/202344s001lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2013/202344Orig1s001ltr.pdf

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
10/13/2020 SUPPL-15

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/202344s015lbl.pdf
06/08/2020 SUPPL-13

Labeling-Medication Guide

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/202344s013lbl.pdf
06/08/2020 SUPPL-13

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/202344s013lbl.pdf
12/30/2016 SUPPL-11

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/202344s011lbl.pdf
04/08/2015 SUPPL-8

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/202344s008lbl.pdf
02/26/2015 SUPPL-7

Labeling-Container/Carton Labels

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/202344s007lbl.pdf
08/02/2013 SUPPL-2

Manufacturing (CMC)

Label (PDF)

This supplement type does not usually require new labeling.

https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/202344s002lbl.pdf
04/19/2013 SUPPL-1

Labeling-Container/Carton Labels

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/202344s001lbl.pdf
04/19/2013 SUPPL-1

Labeling-Medication Guide

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/202344s001lbl.pdf
04/19/2013 SUPPL-1

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/202344s001lbl.pdf
03/12/2012 ORIG-1 Approval

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/202344s000lbl.pdf
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