Tizanidine - 52125-390-02 - (Tizanidine)

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Drug Information of Tizanidine

Product NDC: 52125-390
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: 52125-390
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076286
Marketing Category: ANDA
Start Marketing Date: 20130219

Package Information of Tizanidine

Package NDC: 52125-390-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-390-02)

NDC Information of Tizanidine

NDC Code 52125-390-02
Proprietary Name Tizanidine
Package Description 30 TABLET in 1 BLISTER PACK (52125-390-02)
Product NDC 52125-390
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tizanidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130219
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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