Tizanidine - 63629-3209-7 - (Tizanidine)

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Drug Information of Tizanidine

Product NDC: 63629-3209
Proprietary Name: Tizanidine
Non Proprietary Name: Tizanidine
Active Ingredient(s): 2    mg/1 & nbsp;   Tizanidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Tizanidine

Product NDC: 63629-3209
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076286
Marketing Category: ANDA
Start Marketing Date: 20020703

Package Information of Tizanidine

Package NDC: 63629-3209-7
Package Description: 28 TABLET in 1 BOTTLE (63629-3209-7)

NDC Information of Tizanidine

NDC Code 63629-3209-7
Proprietary Name Tizanidine
Package Description 28 TABLET in 1 BOTTLE (63629-3209-7)
Product NDC 63629-3209
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 Bryant Ranch Prepack
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


General Information