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
CARAFATE از شرکت ALLERGAN
   New Drug Application (NDA): 018333
    
Company: ALLERGAN                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                            
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS | 
|---|---|---|---|---|---|---|---|
| CARAFATE | SUCRALFATE | 1GM | 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 | 
|---|---|---|---|---|---|---|---|
| 10/30/1981 | 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 | 
|---|---|---|---|---|---|
| 03/04/2013 | SUPPL-34 | Labeling-Package Insert | 
 https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/018333s034,019183s016lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2013/018333Orig1s034,019183Orig1s016ltr.pdf  | 
||
| 04/26/2007 | SUPPL-32 | Labeling | 
 https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/018333s032lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2007/018333s032ltr.pdf  | 
||
| 11/29/1995 | SUPPL-29 | Manufacturing (CMC)-Packaging | 
 Label is not available on this site.  | 
||
| 08/15/1995 | SUPPL-28 | Manufacturing (CMC)-Packaging | 
 Label is not available on this site.  | 
||
| 07/14/1994 | SUPPL-27 | Labeling | 
 Label is not available on this site.  | 
||
| 12/28/1992 | SUPPL-26 | Labeling | 
 Label is not available on this site.  | 
||
| 02/12/1991 | SUPPL-25 | Labeling | 
 Label is not available on this site.  | 
||
| 10/05/1990 | SUPPL-24 | Manufacturing (CMC)-Control | 
 Label is not available on this site.  | 
||
| 05/11/1990 | SUPPL-23 | Labeling | 
 Label is not available on this site.  | 
||
| 12/16/1988 | SUPPL-22 | Manufacturing (CMC)-Packaging | 
 Label is not available on this site.  | 
||
| 05/05/1988 | SUPPL-18 | Manufacturing (CMC)-Packaging | 
 Label is not available on this site.  | 
||
| 12/19/1988 | SUPPL-17 | Labeling | 
 Label is not available on this site.  | 
||
| 07/02/1986 | SUPPL-14 | Labeling | 
 Label is not available on this site.  | 
||
| 08/05/1987 | SUPPL-12 | Manufacturing (CMC)-Control | 
 Label is not available on this site.  | 
||
| 09/24/1985 | SUPPL-11 | Manufacturing (CMC)-Packaging | 
 Label is not available on this site.  | 
||
| 08/05/1987 | SUPPL-10 | Manufacturing (CMC)-Control | 
 Label is not available on this site.  | 
||
| 05/11/1990 | SUPPL-9 | Efficacy-New Indication | 
 Label is not available on this site.  | 
||
| 05/14/1985 | SUPPL-8 | Labeling | 
 Label is not available on this site.  | 
||
| 09/24/1984 | SUPPL-6 | Labeling | 
 Label is not available on this site.  | 
||
| 04/22/1983 | SUPPL-5 | Labeling | 
 Label is not available on this site.  | 
||
| 06/01/1983 | SUPPL-4 | Manufacturing (CMC)-Packaging | 
 Label is not available on this site.  | 
||
| 06/09/1983 | SUPPL-3 | Manufacturing (CMC)-Packaging | 
 Label is not available on this site.  | 
||
| 08/16/1982 | SUPPL-2 | Labeling | 
 Label is not available on this site.  | 
||
| 03/09/1982 | SUPPL-1 | Manufacturing (CMC)-Packaging | 
 Label is not available on this site.  | 
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert  | 
Note | Url | 
|---|---|---|---|---|---|
| 03/04/2013 | SUPPL-34 | 
 Labeling-Package Insert  | 
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/018333s034,019183s016lbl.pdf | |
| 04/26/2007 | SUPPL-32 | 
 Labeling  | 
Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/018333s032lbl.pdf | 
CARAFATE
TABLET;ORAL; 1GM
TE Code = AB
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company | 
|---|---|---|---|---|---|---|---|---|
| CARAFATE | SUCRALFATE | 1GM | TABLET;ORAL | Prescription | Yes | AB | 018333 | ALLERGAN | 
| SUCRALFATE | SUCRALFATE | 1GM | TABLET;ORAL | Prescription | No | AB | 074415 | NOSTRUM LABS INC | 
| SUCRALFATE | SUCRALFATE | 1GM | TABLET;ORAL | Prescription | No | AB | 070848 | TEVA | 
                
                  
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
                                                
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