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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 021720

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ARICEPT ODT (DONEPEZIL HYDROCHLORIDE)
5MG
Marketing Status: Discontinued
Active Ingredient: DONEPEZIL HYDROCHLORIDE
Proprietary Name: ARICEPT ODT
Dosage Form; Route of Administration: TABLET, ORALLY DISINTEGRATING; ORAL
Strength: 5MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N021720
Product Number: 001
Approval Date: Oct 18, 2004
Applicant Holder Full Name: EISAI INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
ARICEPT ODT (DONEPEZIL HYDROCHLORIDE)
10MG
Marketing Status: Discontinued
Active Ingredient: DONEPEZIL HYDROCHLORIDE
Proprietary Name: ARICEPT ODT
Dosage Form; Route of Administration: TABLET, ORALLY DISINTEGRATING; ORAL
Strength: 10MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N021720
Product Number: 002
Approval Date: Oct 18, 2004
Applicant Holder Full Name: EISAI INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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