Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 065082
Company: SUN PHARM INDS LTD
Company: SUN PHARM INDS LTD
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
CEFPODOXIME PROXETIL | CEFPODOXIME PROXETIL | EQ 50MG BASE/5ML | FOR SUSPENSION;ORAL | Discontinued | None | No | No |
CEFPODOXIME PROXETIL | CEFPODOXIME PROXETIL | EQ 100MG BASE/5ML | FOR SUSPENSION;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 |
---|---|---|---|---|---|---|---|
05/31/2002 | ORIG-1 | Approval |
Letter (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2002/65082ltr.pdf |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
04/25/2008 | SUPPL-10 | Labeling |
Label is not available on this site. |
||
07/12/2004 | SUPPL-4 | Labeling |
Label is not available on this site. |