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
ALAMAST از شرکت SANTEN
   New Drug Application (NDA): 021079
    
Company: SANTEN                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                              
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS | 
|---|---|---|---|---|---|---|---|
| ALAMAST | PEMIROLAST POTASSIUM | 0.1% | SOLUTION/DROPS;OPHTHALMIC | Discontinued | None | No | 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 | 
|---|---|---|---|---|---|---|---|
| 09/24/1999 | ORIG-1 | Approval | Type 1 – New Molecular Entity | PRIORITY | 
 |         https://www.accessdata.fda.gov/drugsatfda_docs/label/2000/21079lbl.pdf | 
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url | 
|---|---|---|---|---|---|
| 02/15/2013 | SUPPL-14 | Manufacturing (CMC) | Label is not available on this site. | ||
| 05/12/2005 | SUPPL-8 | Labeling | https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/021079s006,008lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/021079s006,008ltr.pdf | ||
| 05/12/2005 | SUPPL-6 | Labeling | https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/021079s006,008lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/021079s006,008ltr.pdf | ||
| 05/03/2002 | SUPPL-5 | Manufacturing (CMC)-Packaging | Label is not available on this site. | ||
| 02/20/2002 | SUPPL-4 | Manufacturing (CMC)-Control | Label is not available on this site. | ||
| 12/12/2000 | SUPPL-2 | Manufacturing (CMC) | Label is not available on this site. | ||
| 05/26/2000 | SUPPL-1 | Manufacturing (CMC)-Control | Label is not available on this site. | 
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url | 
|---|---|---|---|---|---|
| 05/12/2005 | SUPPL-8 | Labeling | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/021079s006,008lbl.pdf | |
| 05/12/2005 | SUPPL-6 | Labeling | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2005/021079s006,008lbl.pdf | |
| 09/24/1999 | ORIG-1 | Approval | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2000/21079lbl.pdf | 
 
                 
                   
                                                 
                                                 
                                                 
                                                 
                                                 
                                                 
                                                 
                                                 
                                                 
                                                 
                                                 
                                                 
                                                 
                                                 
                                                 
                                                
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