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TIZANIDINE HYDROCHLORIDE - 35356-662-90 - (TIZANIDINE HYDROCHLORIDE)

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Drug Information of TIZANIDINE HYDROCHLORIDE

Product NDC: 35356-662
Proprietary Name: TIZANIDINE HYDROCHLORIDE
Non Proprietary Name: TIZANIDINE HYDROCHLORIDE
Active Ingredient(s): 2    mg/1 & nbsp;   TIZANIDINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of TIZANIDINE HYDROCHLORIDE

Product NDC: 35356-662
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076347
Marketing Category: ANDA
Start Marketing Date: 20070206

Package Information of TIZANIDINE HYDROCHLORIDE

Package NDC: 35356-662-90
Package Description: 90 TABLET in 1 BOTTLE (35356-662-90)

NDC Information of TIZANIDINE HYDROCHLORIDE

NDC Code 35356-662-90
Proprietary Name TIZANIDINE HYDROCHLORIDE
Package Description 90 TABLET in 1 BOTTLE (35356-662-90)
Product NDC 35356-662
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TIZANIDINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070206
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name TIZANIDINE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of TIZANIDINE HYDROCHLORIDE


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