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Nexiclon XR - 27808-029-01 - (Clonidine)

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Drug Information of Nexiclon XR

Product NDC: 27808-029
Proprietary Name: Nexiclon XR
Non Proprietary Name: Clonidine
Active Ingredient(s): .09    mg/mL & nbsp;   Clonidine
Administration Route(s): ORAL
Dosage Form(s): FOR SUSPENSION, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Nexiclon XR

Product NDC: 27808-029
Labeler Name: Tris Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022499
Marketing Category: NDA
Start Marketing Date: 20101217

Package Information of Nexiclon XR

Package NDC: 27808-029-01
Package Description: 118 mL in 1 BOTTLE, PLASTIC (27808-029-01)

NDC Information of Nexiclon XR

NDC Code 27808-029-01
Proprietary Name Nexiclon XR
Package Description 118 mL in 1 BOTTLE, PLASTIC (27808-029-01)
Product NDC 27808-029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine
Dosage Form Name FOR SUSPENSION, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101217
Marketing Category Name NDA
Labeler Name Tris Pharma, Inc.
Substance Name CLONIDINE
Strength Number .09
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Nexiclon XR


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