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
COSOPT از شرکت AKORN
New Drug Application (NDA): 020869
Company: AKORN
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
COSOPT | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | 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 |
---|---|---|---|---|---|---|---|
04/07/1998 | ORIG-1 | Approval |
Type 4 – New Combination |
STANDARD |
|
https://www.accessdata.fda.gov/drugsatfda_docs/label/1998/20869lbl.pdf |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
11/23/2020 | SUPPL-42 | Labeling-Patient Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/020869s042lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/020869Orig1s042ltr.pdf |
||
07/31/2015 | SUPPL-40 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/020869s040lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2015/020869Orig1s040ltr.pdf |
||
06/18/2010 | SUPPL-36 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/020869s036lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2010/020869s036ltr.pdf |
||
10/22/2008 | SUPPL-34 | Labeling |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/020869s034lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2008/020869s034ltr.pdf |
||
08/09/2006 | SUPPL-30 | Labeling |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/020869s030lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2006/020869s030LTR.pdf |
||
04/26/2006 | SUPPL-28 | Labeling |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/020869s026s028lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2006/020869s026, s028LTR.pdf |
||
04/26/2006 | SUPPL-26 | Labeling |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/020869s026s028lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2006/020869s026, s028LTR.pdf |
||
12/09/2005 | SUPPL-22 | Labeling |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/020869s022lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/020869s022ltr.pdf |
||
03/28/2005 | SUPPL-20 | Labeling |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/020869s020lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/020869s020ltr.pdf |
||
12/06/2002 | SUPPL-15 | Manufacturing (CMC)-Packaging |
Label is not available on this site. |
||
05/16/2002 | SUPPL-13 | Manufacturing (CMC) |
Label is not available on this site. |
||
04/23/2002 | SUPPL-12 | Labeling |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2002/20869s12lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2002/20869s012.pdf |
||
08/28/2002 | SUPPL-11 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
12/04/2001 | SUPPL-10 | Manufacturing (CMC) |
Label is not available on this site. |
||
12/04/2001 | SUPPL-9 | Manufacturing (CMC) |
Label is not available on this site. |
||
07/24/2001 | SUPPL-8 | Manufacturing (CMC) |
Label is not available on this site. |
||
07/19/2001 | SUPPL-7 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
08/24/2000 | SUPPL-6 | Labeling |
Label is not available on this site. |
||
11/21/2000 | SUPPL-5 | Manufacturing (CMC) |
Label is not available on this site. |
||
01/23/2000 | SUPPL-3 | Labeling |
Label is not available on this site. |
||
11/09/2000 | SUPPL-2 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
01/04/1999 | SUPPL-1 | Labeling |
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/nda/99/20-869-s-001_cosopt.pdf |
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
---|---|---|---|---|---|
11/23/2020 | SUPPL-42 |
Labeling-Patient Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/020869s042lbl.pdf | |
07/31/2015 | SUPPL-40 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/020869s040lbl.pdf | |
06/18/2010 | SUPPL-36 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/020869s036lbl.pdf | |
10/22/2008 | SUPPL-34 |
Labeling |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/020869s034lbl.pdf | |
08/09/2006 | SUPPL-30 |
Labeling |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/020869s030lbl.pdf | |
04/26/2006 | SUPPL-28 |
Labeling |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/020869s026s028lbl.pdf | |
04/26/2006 | SUPPL-26 |
Labeling |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/020869s026s028lbl.pdf | |
12/09/2005 | SUPPL-22 |
Labeling |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/020869s022lbl.pdf | |
03/28/2005 | SUPPL-20 |
Labeling |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/020869s020lbl.pdf | |
04/23/2002 | SUPPL-12 |
Labeling |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2002/20869s12lbl.pdf | |
04/07/1998 | ORIG-1 | Approval | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/1998/20869lbl.pdf |
COSOPT
SOLUTION/DROPS;OPHTHALMIC; EQ 2% BASE;EQ 0.5% BASE
TE Code = AT
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
COSOPT | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | Yes | AT | 020869 | AKORN |
COSOPT PF | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | Yes | AT | 202667 | AKORN |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 077847 | AKORN |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 203058 | AKORN |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 213099 | ALEMBIC PHARMS LTD |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 207629 | AUROBINDO PHARMA LTD |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 207630 | AUROBINDO PHARMA LTD |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 090037 | BAUSCH AND LOMB |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 205295 | FDC LTD |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 078749 | SANDOZ |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 090604 | SANDOZ INC |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 207523 | SOMERSET |
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE | DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE | EQ 2% BASE;EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC | Prescription | No | AT | 078704 | TEVA PHARMS |
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