Tizanidine - 54868-4964-3 - (Tizanidine)

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Drug Information of Tizanidine

Product NDC: 54868-4964
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: 54868-4964
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076286
Marketing Category: ANDA
Start Marketing Date: 20040303

Package Information of Tizanidine

Package NDC: 54868-4964-3
Package Description: 90 TABLET in 1 BOTTLE (54868-4964-3)

NDC Information of Tizanidine

NDC Code 54868-4964-3
Proprietary Name Tizanidine
Package Description 90 TABLET in 1 BOTTLE (54868-4964-3)
Product NDC 54868-4964
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tizanidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040303
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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