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BENICAR از شرکت DAIICHI SANKYO

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BENICAR از شرکت DAIICHI SANKYO

New Drug Application (NDA): 021286

Company: DAIICHI SANKYO

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BENICAR OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription

AB

Yes No
BENICAR OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription

AB

Yes No
BENICAR OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription

AB

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
04/25/2002 ORIG-1 Approval

Type 1 – New Molecular Entity

STANDARD

Label (PDF)

Letter (PDF)

Review

https://www.accessdata.fda.gov/drugsatfda_docs/label/2002/21286lbl.pdf
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2002/21286.pdf
https://www.accessdata.fda.gov/drugsatfda_docs/nda/2002/21-286_Benicar.cfm

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
10/17/2019 SUPPL-40 Labeling

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/021286s040lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/021286Orig1s040ltr.pdf

11/01/2016 SUPPL-36 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/021286s036lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/021286Orig1s036ltr.pdf

07/08/2016 SUPPL-35 Manufacturing (CMC)

Label is not available on this site.

06/10/2016 SUPPL-34 Manufacturing (CMC)

Label is not available on this site.

09/23/2014 SUPPL-32 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021286s032lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/021286Orig1s032ltr.pdf

06/27/2014 SUPPL-31 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021286s031lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/021286Orig1s031ltr.pdf

06/13/2014 SUPPL-30 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021286s030lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/021286Orig1s030ltr.pdf

07/03/2014 SUPPL-29 Manufacturing (CMC)

Label is not available on this site.

10/07/2014 SUPPL-28 Manufacturing (CMC)

Label is not available on this site.

07/03/2013 SUPPL-27 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/021286s027lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2013/021286Orig1s027ltr.pdf

12/11/2012 SUPPL-26 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021286s026lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/021286Orig1s026ltr_r.pdf

09/28/2012 SUPPL-25 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021286s025lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/021286Orig1s025ltr.pdf

02/01/2013 SUPPL-24 Manufacturing (CMC)

Label is not available on this site.

03/29/2012 SUPPL-23 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021286s023lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/021286s023ltr.pdf

02/15/2012 SUPPL-21 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021286s021lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/021286s021ltr.pdf

06/06/2011 SUPPL-20 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/021286s020lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2011/021286s020ltr.pdf

05/19/2011 SUPPL-19 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/021286s019lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2011/021286s019ltr.pdf

02/04/2010 SUPPL-18 Efficacy-New Patient Population

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/021286s018lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2010/021286s018ltr.pdf

09/26/2007 SUPPL-12 Labeling

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2007/021286s012ltr.pdf

07/13/2005 SUPPL-10 Labeling

Label (PDF)

Letter (PDF)

Review (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/021286s010lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/021286s010ltr.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/nda/2005/021286Orig1s010.pdf

11/12/2004 SUPPL-6 Labeling

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2004/21286s006ltr.pdf

02/12/2003 SUPPL-2 Labeling

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2003/21286slr002ltr.pdf

10/25/2002 SUPPL-1 Labeling

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2002/21286slr001ltr.pdf

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
10/17/2019 SUPPL-40

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/021286s040lbl.pdf
11/01/2016 SUPPL-36

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/021286s036lbl.pdf
09/23/2014 SUPPL-32

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021286s032lbl.pdf
06/27/2014 SUPPL-31

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021286s031lbl.pdf
06/13/2014 SUPPL-30

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021286s030lbl.pdf
07/03/2013 SUPPL-27

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/021286s027lbl.pdf
12/11/2012 SUPPL-26

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021286s026lbl.pdf
09/28/2012 SUPPL-25

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021286s025lbl.pdf
03/29/2012 SUPPL-23

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021286s023lbl.pdf
02/15/2012 SUPPL-21

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021286s021lbl.pdf
06/06/2011 SUPPL-20

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/021286s020lbl.pdf
05/19/2011 SUPPL-19

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/021286s019lbl.pdf
02/04/2010 SUPPL-18

Efficacy-New Patient Population

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/021286s018lbl.pdf
07/13/2005 SUPPL-10

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/021286s010lbl.pdf
04/25/2002 ORIG-1 Approval

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2002/21286lbl.pdf

BENICAR

TABLET;ORAL; 5MG

TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
BENICAR OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription Yes AB 021286 DAIICHI SANKYO
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 207662 ACCORD HLTHCARE
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 203012 ALEMBIC PHARMS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 206763 ALKEM LABS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 204798 AUROBINDO PHARMA LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 203281 GLENMARK PHARMS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 204814 MACLEODS PHARMS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 206372 MICRO LABS
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 210552 QILU
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 090237 SANDOZ INC
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 208130 SCIEGEN PHARMS INC
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 211049 SUNSHINE
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 202375 TORRENT
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 207135 UMEDICA LABS PVT LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 5MG TABLET;ORAL Prescription No AB 205192 ZYDUS PHARMS

TABLET;ORAL; 20MG

TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
BENICAR OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription Yes AB 021286 DAIICHI SANKYO
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 207662 ACCORD HLTHCARE
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 203012 ALEMBIC PHARMS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 206763 ALKEM LABS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 204798 AUROBINDO PHARMA LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 203281 GLENMARK PHARMS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 204814 MACLEODS PHARMS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 206372 MICRO LABS
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 210552 QILU
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 090237 SANDOZ INC
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 208130 SCIEGEN PHARMS INC
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 211049 SUNSHINE
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 202375 TORRENT
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 207135 UMEDICA LABS PVT LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 20MG TABLET;ORAL Prescription No AB 205192 ZYDUS PHARMS

TABLET;ORAL; 40MG

TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
BENICAR OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription Yes AB 021286 DAIICHI SANKYO
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 207662 ACCORD HLTHCARE
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 203012 ALEMBIC PHARMS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 206763 ALKEM LABS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 204798 AUROBINDO PHARMA LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 203281 GLENMARK PHARMS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 204814 MACLEODS PHARMS LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 206372 MICRO LABS
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 210552 QILU
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 090237 SANDOZ INC
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 208130 SCIEGEN PHARMS INC
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 211049 SUNSHINE
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 202375 TORRENT
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 207135 UMEDICA LABS PVT LTD
OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL 40MG TABLET;ORAL Prescription No AB 205192 ZYDUS PHARMS
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