Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 021997
Company: MYLAN SPECIALITY LP
Company: MYLAN SPECIALITY LP
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
EDLUAR | ZOLPIDEM TARTRATE | 5MG | TABLET;SUBLINGUAL | Prescription | AB | Yes | No |
EDLUAR | ZOLPIDEM TARTRATE | 10MG | TABLET;SUBLINGUAL | 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 |
---|---|---|---|---|---|---|---|
03/13/2009 | ORIG-1 | Approval | Type 3 - New Dosage Form | STANDARD |
Label (PDF)
Letter (PDF) Review Summary Review |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/021997lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2009/021997s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2009/021997s000TOC.cfm https://www.accessdata.fda.gov/drugsatfda_docs/nda/2009/021997s000TOC.cfm |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
08/18/2019 | SUPPL-11 | Labeling-Medication Guide |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/021997s011lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/021997Orig1s011ltr.pdf | |
02/06/2019 | SUPPL-10 | Labeling-Package Insert |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/021997s010lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/021997Orig1s010ltr.pdf | |
10/24/2018 | SUPPL-8 | Labeling-Package Insert |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/021997s008lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/021997Orig1s008ltr.pdf | |
10/29/2014 | SUPPL-6 | Labeling-Container/Carton Labels, Labeling-Medication Guide |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021997s006lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/021997Orig1s006ltr.pdf | |
04/19/2013 | SUPPL-5 | Labeling-Package Insert |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/021997s005lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2013/021997Orig1s005ltr.pdf | |
08/10/2011 | SUPPL-3 | REMS-Modified |
Letter (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2011/021997s003ltr.pdf |
12/17/2010 | SUPPL-2 | REMS-Modified |
Letter (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2010/021997s002ltr.pdf |
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
---|---|---|---|---|---|
08/18/2019 | SUPPL-11 | Labeling-Medication Guide | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/021997s011lbl.pdf | |
02/06/2019 | SUPPL-10 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/021997s010lbl.pdf | |
10/24/2018 | SUPPL-8 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/021997s008lbl.pdf | |
10/29/2014 | SUPPL-6 | Labeling-Container/Carton Labels | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021997s006lbl.pdf | |
10/29/2014 | SUPPL-6 | Labeling-Medication Guide | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021997s006lbl.pdf | |
04/19/2013 | SUPPL-5 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/021997s005lbl.pdf | |
03/13/2009 | ORIG-1 | Approval | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/021997lbl.pdf |
EDLUAR
TABLET;SUBLINGUAL; 5MG
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
EDLUAR | ZOLPIDEM TARTRATE | 5MG | TABLET;SUBLINGUAL | Prescription | Yes | AB | 021997 | MYLAN SPECIALITY LP |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 5MG | TABLET;SUBLINGUAL | Prescription | No | AB | 201509 | ENDO OPERATIONS |
TABLET;SUBLINGUAL; 10MG
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
EDLUAR | ZOLPIDEM TARTRATE | 10MG | TABLET;SUBLINGUAL | Prescription | Yes | AB | 021997 | MYLAN SPECIALITY LP |
ZOLPIDEM TARTRATE | ZOLPIDEM TARTRATE | 10MG | TABLET;SUBLINGUAL | Prescription | No | AB | 201509 | ENDO OPERATIONS |