Tizanidine - 43063-455-20 - (Tizanidine)

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Drug Information of Tizanidine

Product NDC: 43063-455
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: 43063-455
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076286
Marketing Category: ANDA
Start Marketing Date: 20020703

Package Information of Tizanidine

Package NDC: 43063-455-20
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (43063-455-20)

NDC Information of Tizanidine

NDC Code 43063-455-20
Proprietary Name Tizanidine
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (43063-455-20)
Product NDC 43063-455
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tizanidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020703
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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