Tizanidine - 50436-6756-4 - (Tizanidine)

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Drug Information of Tizanidine

Product NDC: 50436-6756
Proprietary Name: Tizanidine
Non Proprietary Name: Tizanidine
Active Ingredient(s): 4    mg/1 & nbsp;   Tizanidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Tizanidine

Product NDC: 50436-6756
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076286
Marketing Category: ANDA
Start Marketing Date: 20020703

Package Information of Tizanidine

Package NDC: 50436-6756-4
Package Description: 120 TABLET in 1 BOTTLE (50436-6756-4)

NDC Information of Tizanidine

NDC Code 50436-6756-4
Proprietary Name Tizanidine
Package Description 120 TABLET in 1 BOTTLE (50436-6756-4)
Product NDC 50436-6756
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tizanidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020703
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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 Tizanidine


General Information