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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 074672
Company: I3 PHARMS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
SELEGILINE HYDROCHLORIDE SELEGILINE HYDROCHLORIDE 5MG TABLET;ORAL Prescription AB 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
04/01/1997 ORIG-1 Approval

Label is not available on this site.

SELEGILINE HYDROCHLORIDE

TABLET;ORAL; 5MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
SELEGILINE HYDROCHLORIDE SELEGILINE HYDROCHLORIDE 5MG TABLET;ORAL Prescription No AB 074871 APOTEX INC
SELEGILINE HYDROCHLORIDE SELEGILINE HYDROCHLORIDE 5MG TABLET;ORAL Prescription No AB 074672 I3 PHARMS
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