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
AMBIEN از شرکت SANOFI AVENTIS US
New Drug Application (NDA): 019908
Company: SANOFI AVENTIS US
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
AMBIEN | ZOLPIDEM TARTRATE | 5MG | TABLET;ORAL | Prescription |
AB |
Yes | No |
AMBIEN | ZOLPIDEM TARTRATE | 10MG | 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 |
---|---|---|---|---|---|---|---|
12/16/1992 | ORIG-1 | Approval |
Type 1 – New Molecular Entity |
STANDARD |
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/nda/pre96/019908_S000_AmbienTOC.cfm |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
08/18/2019 | SUPPL-46 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/019908s046lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/019908Orig1s046, 021774Orig1s027ltr.pdf |
||
02/06/2019 | SUPPL-45 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/019908s045lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/019908Orig1s045, 021774Orig1s026ltr.pdf |
||
09/14/2018 | SUPPL-42 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/019908s042lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/019908Orig1s042,021774Orig1s023ltr.pdf |
||
03/03/2017 | SUPPL-38 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/019908s038lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2017/019908Orig1s038,021774Orig1s019ltr.pdf |
||
12/02/2016 | SUPPL-37 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019908s037lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/019908Orig1s037,021774Orig1s018ltr.pdf |
||
08/11/2016 | SUPPL-36 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019908s036,021774s017lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/021774Orig1s017,019908Orig1s036ltr.pdf |
||
10/07/2014 | SUPPL-35 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/019908s035,021774s016lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/019908Orig1s035,021774Orig1s016ltr.pdf |
||
04/19/2013 | SUPPL-34 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/019908s032s034,021774s013s015lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2013/019908Orig1s032,s034,021774Orig1s013,s015ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2013/019908Orig1s032,s034,021774Orig1s013,s015review.pdf |
||
06/05/2013 | SUPPL-33 | Manufacturing (CMC) |
Label is not available on this site. |
||
04/19/2013 | SUPPL-32 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/019908s032s034,021774s013s015lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2013/019908Orig1s032,s034,021774Orig1s013,s015ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2013/019908Orig1s032,s034,021774Orig1s013,s015review.pdf |
||
04/14/2010 | SUPPL-29 | Labeling-Package Insert |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/019908s029lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2010/019908s029ltr.pdf |
||
05/07/2008 | SUPPL-27 | Labeling |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/019908s027lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2008/019908s024, s027ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2008/019908Orig1s027.pdf |
||
10/04/2007 | SUPPL-25 | Labeling |
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2007/019908s020s024s025ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2007/019908Orig1s025.pdf |
|
10/04/2007 | SUPPL-24 |
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2007/019908s020s024s025ltr.pdf |
||
03/28/2007 | SUPPL-22 | Efficacy-New Patient Population |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/019908s022lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2007/019908s022ltr.pdf |
||
10/04/2007 | SUPPL-20 | Labeling |
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2007/019908s020s024s025ltr.pdf |
|
09/25/2002 | SUPPL-15 | Manufacturing (CMC) |
Label is not available on this site. |
||
05/21/2002 | SUPPL-14 | Manufacturing (CMC) |
Label is not available on this site. |
||
01/15/2002 | SUPPL-13 | Manufacturing (CMC) |
Label is not available on this site. |
||
11/15/2001 | SUPPL-12 | Manufacturing (CMC) |
Label is not available on this site. |
||
05/04/2001 | SUPPL-11 | Manufacturing (CMC) |
Label is not available on this site. |
||
04/13/2001 | SUPPL-10 | Manufacturing (CMC) |
Label is not available on this site. |
||
12/01/1999 | SUPPL-9 | Labeling |
Label is not available on this site. |
||
04/18/1996 | SUPPL-5 | Manufacturing (CMC) |
Label is not available on this site. |
||
10/04/1995 | SUPPL-4 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
01/09/1995 | SUPPL-3 | Manufacturing (CMC)-Packaging |
Label is not available on this site. |
||
07/14/1995 | SUPPL-2 | Labeling |
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/nda/pre96/019908_S002_AMBIEN_AP.pdf |
|
07/14/1995 | SUPPL-1 | Labeling |
Label is not available on this site. |
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
---|---|---|---|---|---|
08/18/2019 | SUPPL-46 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/019908s046lbl.pdf | |
02/06/2019 | SUPPL-45 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/019908s045lbl.pdf | |
09/14/2018 | SUPPL-42 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/019908s042lbl.pdf | |
03/03/2017 | SUPPL-38 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/019908s038lbl.pdf | |
12/02/2016 | SUPPL-37 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019908s037lbl.pdf | |
08/11/2016 | SUPPL-36 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019908s036,021774s017lbl.pdf | |
10/07/2014 | SUPPL-35 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/019908s035,021774s016lbl.pdf | |
04/19/2013 | SUPPL-34 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/019908s032s034,021774s013s015lbl.pdf | |
04/19/2013 | SUPPL-32 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/019908s032s034,021774s013s015lbl.pdf | |
04/14/2010 | SUPPL-29 |
Labeling-Package Insert |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/019908s029lbl.pdf | |
05/07/2008 | SUPPL-27 |
Labeling |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/019908s027lbl.pdf | |
03/28/2007 | SUPPL-22 |
Efficacy-New Patient Population |
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/019908s022lbl.pdf |
AMBIEN
TABLET;ORAL; 5MG
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
AMBIEN | ZOLPIDEM TARTRATE | 5MG | TABLET;ORAL | Prescription | Yes | AB | 019908 | SANOFI AVENTIS US |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 5MG | TABLET;ORAL | Prescription | No | AB | 077214 | ACME LABS |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 5MG | TABLET;ORAL | Prescription | No | AB | 077884 | APOTEX INC |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 5MG | TABLET;ORAL | Prescription | No | AB | 078413 | AUROBINDO PHARMA |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 5MG | TABLET;ORAL | Prescription | No | AB | 077388 | CIPLA LTD |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 5MG | TABLET;ORAL | Prescription | No | AB | 078184 | INVAGEN PHARMS |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 5MG | TABLET;ORAL | Prescription | No | AB | 077322 | SANDOZ INC |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 5MG | TABLET;ORAL | Prescription | No | AB | 076410 | TEVA |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 5MG | TABLET;ORAL | Prescription | No | AB | 077903 | TORRENT PHARMS |
TABLET;ORAL; 10MG
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
AMBIEN | ZOLPIDEM TARTRATE | 10MG | TABLET;ORAL | Prescription | Yes | AB | 019908 | SANOFI AVENTIS US |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 10MG | TABLET;ORAL | Prescription | No | AB | 077214 | ACME LABS |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 10MG | TABLET;ORAL | Prescription | No | AB | 077884 | APOTEX INC |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 10MG | TABLET;ORAL | Prescription | No | AB | 078413 | AUROBINDO PHARMA |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 10MG | TABLET;ORAL | Prescription | No | AB | 077388 | CIPLA LTD |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 10MG | TABLET;ORAL | Prescription | No | AB | 078184 | INVAGEN PHARMS |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 10MG | TABLET;ORAL | Prescription | No | AB | 077322 | SANDOZ INC |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 10MG | TABLET;ORAL | Prescription | No | AB | 076410 | TEVA |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 10MG | TABLET;ORAL | Prescription | No | AB | 077903 | TORRENT PHARMS |
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