Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 076844
Company: HIKMA
Company: HIKMA
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| ZIDOVUDINE | ZIDOVUDINE | 300MG | 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 |
|---|---|---|---|---|---|---|---|
| 09/19/2005 | ORIG-1 | Approval |
Letter (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/076844ltr.pdf |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 10/31/2012 | SUPPL-6 | Labeling-Package Insert |
Label is not available on this site. |
||
| 04/12/2011 | SUPPL-5 | Labeling-Package Insert |
Label is not available on this site. |
||
| 04/08/2009 | SUPPL-4 | Labeling |
Label is not available on this site. |
||
| 05/24/2007 | SUPPL-2 | Labeling |
Label is not available on this site. |
||
| 04/04/2007 | SUPPL-1 | Labeling |
Label is not available on this site. |