Tizanidine - 0378-0722-01 - (tizanidine)

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Drug Information of Tizanidine

Product NDC: 0378-0722
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: 0378-0722
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076354
Marketing Category: ANDA
Start Marketing Date: 20130321

Package Information of Tizanidine

Package NDC: 0378-0722-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0378-0722-01)

NDC Information of Tizanidine

NDC Code 0378-0722-01
Proprietary Name Tizanidine
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0378-0722-01)
Product NDC 0378-0722
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tizanidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130321
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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