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CARBAGLU از شرکت RECORDATI RARE

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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

CARBAGLU از شرکت RECORDATI RARE

New Drug Application (NDA): 022562

Company: RECORDATI RARE

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CARBAGLU CARGLUMIC ACID 200MG TABLET, FOR SUSPENSION;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
03/18/2010 ORIG-1 Approval

Type 1 – New Molecular Entity

PRIORITY; Orphan

Label (PDF)

Letter (PDF)

Review

https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/022562lbl.pdf
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2010/022562s000ltr.pdf
https://www.accessdata.fda.gov/drugsatfda_docs/nda/2010/022562s000TOC.cfm

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
08/05/2021 SUPPL-13 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/022562s013lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/022562Orig1s013ltr.pdf

08/26/2020 SUPPL-12 Labeling-Package Insert

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/022562Orig1s012ltr.pdf

12/23/2019 SUPPL-11 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/022562s011lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/022562Orig1s011ltr.pdf

01/22/2021 SUPPL-9 Efficacy-New Indication

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/022562s008s009lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/022562Orig1s008, s009ltr.pdf

01/22/2021 SUPPL-8 Efficacy-New Indication

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/022562s008s009lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/022562Orig1s008, s009ltr.pdf

11/16/2017 SUPPL-5 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/022562s005lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2017/022562Orig1s005ltr.pdf

11/05/2015 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

01/23/2014 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

08/05/2013 SUPPL-2 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/022562s002lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2013/022562Orig1s002ltr.pdf

07/22/2013 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
08/05/2021 SUPPL-13

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/022562s013lbl.pdf
01/22/2021 SUPPL-9

Efficacy-New Indication

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/022562s008s009lbl.pdf
01/22/2021 SUPPL-8

Efficacy-New Indication

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/022562s008s009lbl.pdf
12/23/2019 SUPPL-11

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/022562s011lbl.pdf
11/16/2017 SUPPL-5

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/022562s005lbl.pdf
08/05/2013 SUPPL-2

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/022562s002lbl.pdf
03/18/2010 ORIG-1 Approval

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/022562lbl.pdf
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