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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 022500

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NEXICLON XR (CLONIDINE)
EQ 0.17MG BASE
Marketing Status: Prescription
Active Ingredient: CLONIDINE
Proprietary Name: NEXICLON XR
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 0.17MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N022500
Product Number: 001
Approval Date: Dec 3, 2009
Applicant Holder Full Name: ATHENA BIOSCIENCE LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
NEXICLON XR (CLONIDINE)
EQ 0.26MG BASE
Marketing Status: Discontinued
Active Ingredient: CLONIDINE
Proprietary Name: NEXICLON XR
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 0.26MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N022500
Product Number: 002
Approval Date: Dec 3, 2009
Applicant Holder Full Name: ATHENA BIOSCIENCE LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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