0

ACULAR از شرکت ALLERGAN

تصویر پیدا نشد !

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

ACULAR از شرکت ALLERGAN

New Drug Application (NDA): 019700

Company: ALLERGAN

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ACULAR KETOROLAC TROMETHAMINE 0.5% SOLUTION/DROPS;OPHTHALMIC Prescription

AT

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
11/09/1992 ORIG-1 Approval

Type 3 – New Dosage Form

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
06/14/2012 SUPPL-28 Labeling-Package Insert

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/019700s028lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/019700s028ltr.pdf

03/10/2005 SUPPL-24 Labeling

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/19700S023,024lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/19700S023,024ltr.pdf

03/10/2005 SUPPL-23 Manufacturing (CMC)-Packaging

Label (PDF)

Letter (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/19700S023,024lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/19700S023,024ltr.pdf

04/12/2002 SUPPL-22 Manufacturing (CMC)

Label is not available on this site.

04/15/2002 SUPPL-21 Manufacturing (CMC)-Packaging

Label is not available on this site.

12/04/2001 SUPPL-20 Manufacturing (CMC)

Label is not available on this site.

02/08/2002 SUPPL-19 Efficacy-New Patient Population

Label (PDF)

Letter (PDF)

Review (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2002/19700s019lbl.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2002/19700s019ltr.pdf

https://www.accessdata.fda.gov/drugsatfda_docs/nda/2002/019700_S019_ACULAR.pdf

07/16/2001 SUPPL-18 Manufacturing (CMC)

Label (PDF)

https://www.accessdata.fda.gov/drugsatfda_docs/label/2001/19700s18lbl.pdf

04/12/2001 SUPPL-17 Manufacturing (CMC)

Label is not available on this site.

10/02/2000 SUPPL-16 Manufacturing (CMC)

Label is not available on this site.

04/27/2001 SUPPL-14 Labeling

Label is not available on this site.

02/04/1998 SUPPL-13 Manufacturing (CMC)-Control

Label is not available on this site.

05/19/1998 SUPPL-12 Manufacturing (CMC)-Control

Label is not available on this site.

07/21/1997 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

04/30/1997 SUPPL-9 Manufacturing (CMC)-Control

Label is not available on this site.

12/31/1996 SUPPL-7 Efficacy-New Indication

Label is not available on this site.

07/11/1996 SUPPL-6 Manufacturing (CMC)-Control

Label is not available on this site.

09/18/1996 SUPPL-5 Manufacturing (CMC)-Control

Label is not available on this site.

09/18/1996 SUPPL-4 Labeling

Label is not available on this site.

09/18/1996 SUPPL-3 Efficacy-New Dosing Regimen

Label is not available on this site.

03/29/1996 SUPPL-2 Manufacturing (CMC)-Control

Label is not available on this site.

04/14/1994 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
06/14/2012 SUPPL-28

Labeling-Package Insert

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/019700s028lbl.pdf
03/10/2005 SUPPL-24

Labeling

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/19700S023,024lbl.pdf
03/10/2005 SUPPL-23

Manufacturing (CMC)-Packaging

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/19700S023,024lbl.pdf
02/08/2002 SUPPL-19

Efficacy-New Patient Population

Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2002/19700s019lbl.pdf
07/16/2001 SUPPL-18

Manufacturing (CMC)

Label (PDF)

This supplement type does not usually require new labeling.

https://www.accessdata.fda.gov/drugsatfda_docs/label/2001/19700s18lbl.pdf

ACULAR

SOLUTION/DROPS;OPHTHALMIC; 0.5%

TE Code = AT

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
ACULAR KETOROLAC TROMETHAMINE 0.5% SOLUTION/DROPS;OPHTHALMIC Prescription Yes AT 019700 ALLERGAN
KETOROLAC TROMETHAMINE KETOROLAC TROMETHAMINE 0.5% SOLUTION/DROPS;OPHTHALMIC Prescription No AT 078434 AKORN
KETOROLAC TROMETHAMINE KETOROLAC TROMETHAMINE 0.5% SOLUTION/DROPS;OPHTHALMIC Prescription No AT 076109 APOTEX INC
KETOROLAC TROMETHAMINE KETOROLAC TROMETHAMINE 0.5% SOLUTION/DROPS;OPHTHALMIC Prescription No AT 203410 MICRO LABS LTD INDIA
KETOROLAC TROMETHAMINE KETOROLAC TROMETHAMINE 0.5% SOLUTION/DROPS;OPHTHALMIC Prescription No AT 076583 SANDOZ INC
KETOROLAC TROMETHAMINE KETOROLAC TROMETHAMINE 0.5% SOLUTION/DROPS;OPHTHALMIC Prescription No AT 090017 SUN PHARM
برچسب‌ها:

نظرات کاربران