Zanaflex - 10144-606-15 - (tizanidine hydrochloride)

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Drug Information of Zanaflex

Product NDC: 10144-606
Proprietary Name: Zanaflex
Non Proprietary Name: tizanidine hydrochloride
Active Ingredient(s): 6    mg/1 & nbsp;   tizanidine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Zanaflex

Product NDC: 10144-606
Labeler Name: Acorda Therapeutics, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021447
Marketing Category: NDA
Start Marketing Date: 20050404

Package Information of Zanaflex

Package NDC: 10144-606-15
Package Description: 150 CAPSULE in 1 BOTTLE (10144-606-15)

NDC Information of Zanaflex

NDC Code 10144-606-15
Proprietary Name Zanaflex
Package Description 150 CAPSULE in 1 BOTTLE (10144-606-15)
Product NDC 10144-606
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tizanidine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050404
Marketing Category Name NDA
Labeler Name Acorda Therapeutics, Inc.
Substance Name TIZANIDINE HYDROCHLORIDE
Strength Number 6
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Zanaflex


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