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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 209369
Company: RHODES PHARMS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
TAPENTADOL HYDROCHLORIDE TAPENTADOL HYDROCHLORIDE 50MG TABLET;ORAL None (Tentative Approval) None No No
TAPENTADOL HYDROCHLORIDE TAPENTADOL HYDROCHLORIDE 75MG TABLET;ORAL None (Tentative Approval) None No No
TAPENTADOL HYDROCHLORIDE TAPENTADOL HYDROCHLORIDE 100MG TABLET;ORAL None (Tentative Approval) 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
09/14/2017 ORIG-1 Tentative Approval STANDARD

Label is not available on this site.

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