Active Ingredient: SELEGILINE HYDROCHLORIDE
Proprietary Name: SELEGILINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019334
Product Number: 001
Approval Date: Jun 5, 1989
Applicant Holder Full Name: SOMERSET PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information