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Tizanidine Hydrochloride - 60505-2648-3 - (Tizanidine Hydrochloride)

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Drug Information of Tizanidine Hydrochloride

Product NDC: 60505-2648
Proprietary Name: Tizanidine Hydrochloride
Non Proprietary Name: Tizanidine Hydrochloride
Active Ingredient(s): 2    mg/1 & nbsp;   Tizanidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tizanidine Hydrochloride

Product NDC: 60505-2648
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078868
Marketing Category: ANDA
Start Marketing Date: 20120206

Package Information of Tizanidine Hydrochloride

Package NDC: 60505-2648-3
Package Description: 30 CAPSULE, GELATIN COATED in 1 BOTTLE (60505-2648-3)

NDC Information of Tizanidine Hydrochloride

NDC Code 60505-2648-3
Proprietary Name Tizanidine Hydrochloride
Package Description 30 CAPSULE, GELATIN COATED in 1 BOTTLE (60505-2648-3)
Product NDC 60505-2648
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tizanidine Hydrochloride
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20120206
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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 Hydrochloride


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