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tizanidine hydrochloride - 55289-809-60 - (tizanidine hydrochloride)

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Drug Information of tizanidine hydrochloride

Product NDC: 55289-809
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): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of tizanidine hydrochloride

Product NDC: 55289-809
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076280
Marketing Category: ANDA
Start Marketing Date: 20021126

Package Information of tizanidine hydrochloride

Package NDC: 55289-809-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (55289-809-60)

NDC Information of tizanidine hydrochloride

NDC Code 55289-809-60
Proprietary Name tizanidine hydrochloride
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (55289-809-60)
Product NDC 55289-809
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tizanidine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20021126
Marketing Category Name ANDA
Labeler Name PD-Rx 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 hydrochloride


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