Zanaflex - 35356-342-90 - (tizanidine hydrochloride)

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Drug Information of Zanaflex

Product NDC: 35356-342
Proprietary Name: Zanaflex
Non Proprietary Name: tizanidine hydrochloride
Active Ingredient(s): 4    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: 35356-342
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021447
Marketing Category: NDA
Start Marketing Date: 20120328

Package Information of Zanaflex

Package NDC: 35356-342-90
Package Description: 90 CAPSULE in 1 BOTTLE (35356-342-90)

NDC Information of Zanaflex

NDC Code 35356-342-90
Proprietary Name Zanaflex
Package Description 90 CAPSULE in 1 BOTTLE (35356-342-90)
Product NDC 35356-342
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tizanidine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120328
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name TIZANIDINE HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Zanaflex


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