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
CALCIUM DISODIUM VERSENATE از شرکت BAUSCH
   New Drug Application (NDA): 008922
    
Company: BAUSCH                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                              
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS | 
|---|---|---|---|---|---|---|---|
| CALCIUM DISODIUM VERSENATE | EDETATE CALCIUM DISODIUM | 200MG/ML | INJECTABLE;INJECTION | Prescription | 
 None  | 
Yes | Yes | 
| CALCIUM DISODIUM VERSENATE | EDETATE CALCIUM DISODIUM | 500MG | TABLET;ORAL | 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 | 
|---|---|---|---|---|---|---|---|
| 07/16/1953 | ORIG-1 | Approval | 
 Type 1 – New Molecular Entity  | 
 PRIORITY  | 
 
 
  | 
 Label is not available on this site.  | 
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url | 
|---|---|---|---|---|---|
| 06/17/2015 | SUPPL-19 | Manufacturing (CMC) | 
 Label is not available on this site.  | 
||
| 06/21/2013 | SUPPL-18 | Manufacturing (CMC) | 
 Label is not available on this site.  | 
||
| 05/19/2009 | SUPPL-16 | Labeling | 
 https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/008922s016lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2009/008922s016ltr.pdf  | 
||
| 04/12/2002 | SUPPL-15 | Manufacturing (CMC) | 
 Label is not available on this site.  | 
||
| 09/26/1996 | SUPPL-14 | Labeling | 
 Label is not available on this site.  | 
||
| 10/05/1992 | SUPPL-13 | Labeling | 
 Label is not available on this site.  | 
||
| 03/03/1992 | SUPPL-12 | Labeling | 
 Label is not available on this site.  | 
||
| 04/25/1985 | SUPPL-11 | 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 | 
|---|---|---|---|---|---|
| 05/19/2009 | SUPPL-16 | 
 Labeling  | 
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/008922s016lbl.pdf | 
                
                  
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
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