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
ACIPHEX SPRINKLE از شرکت AYTU
   New Drug Application (NDA): 204736
    
Company: AYTU                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS | 
|---|---|---|---|---|---|---|---|
| ACIPHEX SPRINKLE | RABEPRAZOLE SODIUM | 5MG | CAPSULE, DELAYED RELEASE;ORAL | Discontinued | 
 None  | 
Yes | No | 
| ACIPHEX SPRINKLE | RABEPRAZOLE SODIUM | 10MG | CAPSULE, DELAYED RELEASE;ORAL | Discontinued | 
 None  | 
Yes | No | 
Original Approvals or Tentative Approvals
| Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url | 
|---|---|---|---|---|---|---|---|
| 03/26/2013 | ORIG-1 | Approval | 
 Type 3 – New Dosage Form  | 
 PRIORITY  | 
 
  | 
         https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/204736s000lbl.pdf  | 
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url | 
|---|---|---|---|---|---|
| 11/27/2020 | SUPPL-12 | Labeling-Package Insert | 
 https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/204736s012lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/204736Orig1s012ltr.pdf  | 
||
| 06/07/2018 | SUPPL-10 | Labeling-Package Insert | 
 https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/204736s010lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/204736Orig1s010ltr.pdf  | 
||
| 07/27/2017 | SUPPL-8 | Labeling-Package Insert | 
 https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/204736s008lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2017/204736Orig1s008ltr.pdf  | 
||
| 10/24/2016 | SUPPL-7 | Labeling-Package Insert | 
 Label is not available on this site.  | 
 https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/204736Orig1s007ltr.pdf  | 
|
| 10/13/2015 | SUPPL-6 | Manufacturing (CMC) | 
 Label is not available on this site.  | 
||
| 12/19/2014 | SUPPL-5 | Labeling-Medication Guide, Labeling-Package Insert | 
 https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/020973s035204736s005lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/020973Orig1s035,204736Orig1s005ltr.pdf  | 
||
| 10/15/2014 | SUPPL-4 | Labeling-Package Insert | 
 https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/020973s034,204736s004lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/204736Orig1s004,020973Orig1s034ltr.pdf  | 
||
| 04/04/2016 | SUPPL-3 | Labeling-Package Insert | 
 https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/204736s003lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/020973Orig1s033,204736Orig1s003ltr.pdf  | 
||
| 08/28/2013 | 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 | 
|---|---|---|---|---|---|
| 11/27/2020 | SUPPL-12 | 
 Labeling-Package Insert  | 
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/204736s012lbl.pdf | |
| 06/07/2018 | SUPPL-10 | 
 Labeling-Package Insert  | 
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/204736s010lbl.pdf | |
| 07/27/2017 | SUPPL-8 | 
 Labeling-Package Insert  | 
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/204736s008lbl.pdf | |
| 04/04/2016 | SUPPL-3 | 
 Labeling-Package Insert  | 
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/204736s003lbl.pdf | |
| 12/19/2014 | SUPPL-5 | 
 Labeling-Medication Guide  | 
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/020973s035204736s005lbl.pdf | |
| 12/19/2014 | SUPPL-5 | 
 Labeling-Package Insert  | 
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/020973s035204736s005lbl.pdf | |
| 10/15/2014 | SUPPL-4 | 
 Labeling-Package Insert  | 
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/020973s034,204736s004lbl.pdf | |
| 03/26/2013 | ORIG-1 | Approval | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/204736s000lbl.pdf | 
                
                  
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
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