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COPAXONE از شرکت TEVA PHARMS USA

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COPAXONE از شرکت TEVA PHARMS USA

New Drug Application (NDA): 020622

Company: TEVA PHARMS USA

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
COPAXONE GLATIRAMER ACETATE 20MG/VIAL FOR SOLUTION;SUBCUTANEOUS Discontinued

None

No No
COPAXONE GLATIRAMER ACETATE 20MG/ML INJECTABLE;SUBCUTANEOUS Prescription

AP

Yes Yes
COPAXONE GLATIRAMER ACETATE 40MG/ML INJECTABLE;SUBCUTANEOUS Prescription

AP

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
12/20/1996 ORIG-1 Approval

Type 1 – New Molecular Entity

STANDARD; Orphan

Review (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/nda/pre96/020622Orig1s000rev.pdf

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
07/22/2020 SUPPL-110 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/020622s110lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/020622Orig1s110ltr.pdf

05/14/2020 SUPPL-109 Labeling-Container/Carton Labels

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/020622Orig1s109ltr.pdf

12/27/2019 SUPPL-107 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/020622s107lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/020622Orig1s107ltr.pdf

07/19/2019 SUPPL-106 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/020622s106lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/020622Orig1s106ltr.pdf

09/07/2018 SUPPL-104 Labeling-Package Insert, Labeling-Patient Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/020622s104lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/020622Orig1s104ltr.pdf

01/23/2018 SUPPL-102 Labeling-Patient Package Insert, Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/020622s102lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/020622Orig1s102ltr.pdf

11/18/2016 SUPPL-99 Manufacturing (CMC)

Label is not available on this site.

11/15/2016 SUPPL-98 Manufacturing (CMC)

Label is not available on this site.

10/02/2015 SUPPL-96 Manufacturing (CMC)

Label is not available on this site.

12/03/2015 SUPPL-95 Manufacturing (CMC)

Label is not available on this site.

08/03/2015 SUPPL-94 Manufacturing (CMC)

Label is not available on this site.

03/14/2016 SUPPL-93 Manufacturing (CMC)

Label is not available on this site.

01/26/2015 SUPPL-92 Manufacturing (CMC)

Label is not available on this site.

12/06/2013 SUPPL-91 Manufacturing (CMC)

Label is not available on this site.

01/28/2014 SUPPL-89 Efficacy-New Dosing Regimen

Label (PDF)

Letter (PDF)

Review (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/020622s089lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/020622Orig1s089ltr.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/nda/2014/020622Orig1s089.pdf

03/08/2013 SUPPL-87 Manufacturing (CMC)

Label (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020622s087lbl.pdf

09/05/2013 SUPPL-85 Manufacturing (CMC)

Label is not available on this site.

09/05/2013 SUPPL-83 Manufacturing (CMC)

Label is not available on this site.

02/22/2013 SUPPL-79 Manufacturing (CMC)

Label is not available on this site.

02/27/2009 SUPPL-57 Efficacy-New Patient Population

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/020622s057lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2009/020622s057ltr.pdf

08/29/2002 SUPPL-26 Labeling

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2002/20622slr026ltr.pdf

05/20/2002 SUPPL-25 Manufacturing (CMC)

Label is not available on this site.

03/11/2002 SUPPL-24 Manufacturing (CMC)

Label is not available on this site.

02/12/2002 SUPPL-23 Manufacturing (CMC)-Formulation

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2002/20622s23ltr.pdf

06/12/2001 SUPPL-22 Labeling

Label is not available on this site.

02/28/2001 SUPPL-20 Labeling

Label is not available on this site.

02/23/2001 SUPPL-19 Manufacturing (CMC)

Label is not available on this site.

01/25/2001 SUPPL-18 Manufacturing (CMC)-Control

Label is not available on this site.

11/29/1999 SUPPL-17 Manufacturing (CMC)

Label is not available on this site.

09/24/1999 SUPPL-16 Manufacturing (CMC)

Label is not available on this site.

07/12/2001 SUPPL-15 Labeling

Label (PDF)

Review (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2001/20622s15lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/nda/2001/020622_S015_COPAXONE_INJECTION_AP.pdf

08/16/1999 SUPPL-14 Manufacturing (CMC)-Control

Label is not available on this site.

08/16/1999 SUPPL-13 Manufacturing (CMC)

Label is not available on this site.

08/04/1999 SUPPL-12 Manufacturing (CMC)

Label is not available on this site.

08/03/1999 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

07/30/1999 SUPPL-10 Manufacturing (CMC)-Control

Label is not available on this site.

07/06/2000 SUPPL-9 Labeling

Label is not available on this site.

06/28/1999 SUPPL-8 Manufacturing (CMC)

Label is not available on this site.

08/09/2000 SUPPL-7 Labeling

Label is not available on this site.

02/25/1999 SUPPL-6 Manufacturing (CMC)-Control

Label is not available on this site.

02/16/1999 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

07/06/2000 SUPPL-4 Labeling

Label is not available on this site.

01/23/1998 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

01/23/1998 SUPPL-2 Manufacturing (CMC)-Control

Label is not available on this site.

11/04/1997 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
07/22/2020 SUPPL-110

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/020622s110lbl.pdf
12/27/2019 SUPPL-107

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/020622s107lbl.pdf
07/19/2019 SUPPL-106

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/020622s106lbl.pdf
09/07/2018 SUPPL-104

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/020622s104lbl.pdf
09/07/2018 SUPPL-104

Labeling-Patient Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/020622s104lbl.pdf
01/23/2018 SUPPL-102

Labeling-Patient Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/020622s102lbl.pdf
01/23/2018 SUPPL-102

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/020622s102lbl.pdf
01/28/2014 SUPPL-89

Efficacy-New Dosing Regimen

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/020622s089lbl.pdf
03/08/2013 SUPPL-87

Manufacturing (CMC)

Label (PDF)

This supplement type does not usually require new labeling.

https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020622s087lbl.pdf
02/27/2009 SUPPL-57

Efficacy-New Patient Population

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/020622s057lbl.pdf
07/12/2001 SUPPL-15

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2001/20622s15lbl.pdf

COPAXONE

INJECTABLE;SUBCUTANEOUS; 20MG/ML

TE Code = AP

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
COPAXONE GLATIRAMER ACETATE 20MG/ML INJECTABLE;SUBCUTANEOUS Prescription Yes AP 020622 TEVA PHARMS USA
GLATIRAMER ACETATE GLATIRAMER ACETATE 20MG/ML INJECTABLE;SUBCUTANEOUS Prescription No AP 091646 MYLAN
GLATOPA GLATIRAMER ACETATE 20MG/ML INJECTABLE;SUBCUTANEOUS Prescription No AP 090218 SANDOZ INC

INJECTABLE;SUBCUTANEOUS; 40MG/ML

TE Code = AP

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
COPAXONE GLATIRAMER ACETATE 40MG/ML INJECTABLE;SUBCUTANEOUS Prescription Yes AP 020622 TEVA PHARMS USA
GLATIRAMER ACETATE GLATIRAMER ACETATE 40MG/ML INJECTABLE;SUBCUTANEOUS Prescription No AP 206936 MYLAN
GLATOPA GLATIRAMER ACETATE 40MG/ML INJECTABLE;SUBCUTANEOUS Prescription No AP 206921 SANDOZ INC
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