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CATAFLAM از شرکت NOVARTIS

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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

CATAFLAM از شرکت NOVARTIS

New Drug Application (NDA): 020142

Company: NOVARTIS

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CATAFLAM DICLOFENAC POTASSIUM 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** TABLET;ORAL Discontinued

None

Yes No
CATAFLAM DICLOFENAC POTASSIUM 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** TABLET;ORAL Discontinued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
11/24/1993 ORIG-1 Approval

Type 2 – New Active Ingredient

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
04/28/2021 SUPPL-29 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/020142s029lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/020142Orig1s029ltr.pdf

05/09/2016 SUPPL-27 Labeling-Package Insert, Labeling-Medication Guide, Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/020142s027lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/020142Orig1s027ltr.pdf

11/24/2014 SUPPL-26 Manufacturing (CMC)

Label is not available on this site.

02/23/2011 SUPPL-22 Labeling

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/020142s021s022lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2011/020142s021,s022ltr.pdf

02/23/2011 SUPPL-21 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/020142s021s022lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2011/020142s021,s022ltr.pdf

02/25/2009 SUPPL-19 Labeling

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/020142s019lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2009/020142s019ltr.pdf

01/24/2006 SUPPL-17 Labeling

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/020142s017lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2006/020254s016_020142s017_019201s035ltr.pdf

09/19/2002 SUPPL-15 Manufacturing (CMC)-Control

Label is not available on this site.

03/11/2002 SUPPL-14 Manufacturing (CMC)

Label is not available on this site.

07/13/2001 SUPPL-13 Manufacturing (CMC)

Label is not available on this site.

09/15/2000 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

07/10/2000 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

04/22/1999 SUPPL-9 Manufacturing (CMC)-Packaging

Label is not available on this site.

11/12/1997 SUPPL-8 Manufacturing (CMC)-Control

Label is not available on this site.

05/16/1997 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

10/31/2001 SUPPL-6 Labeling

Label is not available on this site.

04/20/1998 SUPPL-5 Labeling

Label is not available on this site.

11/28/1995 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

07/28/1995 SUPPL-3 Labeling

Label is not available on this site.

07/06/1994 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

01/11/1995 SUPPL-1 Manufacturing (CMC)-Control

Label is not available on this site.

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
04/28/2021 SUPPL-29

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/020142s029lbl.pdf
05/09/2016 SUPPL-27

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/020142s027lbl.pdf
05/09/2016 SUPPL-27

Labeling-Medication Guide

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/020142s027lbl.pdf
05/09/2016 SUPPL-27

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/020142s027lbl.pdf
02/23/2011 SUPPL-22

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/020142s021s022lbl.pdf
02/23/2011 SUPPL-21

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/020142s021s022lbl.pdf
02/25/2009 SUPPL-19

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/020142s019lbl.pdf
01/24/2006 SUPPL-17

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/020142s017lbl.pdf
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