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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 021479

ZELAPAR (SELEGILINE HYDROCHLORIDE)
1.25MG
Marketing Status: Prescription
Active Ingredient: SELEGILINE HYDROCHLORIDE
Proprietary Name: ZELAPAR
Dosage Form; Route of Administration: TABLET, ORALLY DISINTEGRATING; ORAL
Strength: 1.25MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N021479
Product Number: 001
Approval Date: Jun 14, 2006
Applicant Holder Full Name: BAUSCH HEALTH US LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
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