Tizanidine - 29300-169-05 - (Tizanidine)

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Drug Information of Tizanidine

Product NDC: 29300-169
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: 29300-169
Labeler Name: Unichem Pharmaceuticals (USA), Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091283
Marketing Category: ANDA
Start Marketing Date: 20130401

Package Information of Tizanidine

Package NDC: 29300-169-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (29300-169-05)

NDC Information of Tizanidine

NDC Code 29300-169-05
Proprietary Name Tizanidine
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (29300-169-05)
Product NDC 29300-169
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tizanidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130401
Marketing Category Name ANDA
Labeler Name Unichem Pharmaceuticals (USA), 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