Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 063017
Company: PUREPAC PHARM
Company: PUREPAC PHARM
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
CEFADROXIL | CEFADROXIL/CEFADROXIL HEMIHYDRATE | EQ 500MG BASE | CAPSULE;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 |
---|---|---|---|---|---|---|---|
01/05/1989 | ORIG-1 | Approval |
Label is not available on this site. |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
08/28/1992 | SUPPL-5 | Labeling |
Label is not available on this site. |
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04/06/1992 | SUPPL-3 | Labeling |
Label is not available on this site. |
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02/03/1992 | SUPPL-2 | Labeling |
Label is not available on this site. |