Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 083688
Company: SANDOZ
Company: SANDOZ
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
PROPOXYPHENE HYDROCHLORIDE | PROPOXYPHENE HYDROCHLORIDE | 65MG | 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 |
---|---|---|---|---|---|---|---|
02/13/1975 | 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 |
---|---|---|---|---|---|
02/14/1983 | SUPPL-7 | Manufacturing (CMC) |
Label is not available on this site. |
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02/14/1983 | SUPPL-6 | Manufacturing (CMC) |
Label is not available on this site. |