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tizanidine hydrochloride - 0185-0034-51 - (tizanidine hydrochloride)

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Drug Information of tizanidine hydrochloride

Product NDC: 0185-0034
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: 0185-0034
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076280
Marketing Category: ANDA
Start Marketing Date: 20021126

Package Information of tizanidine hydrochloride

Package NDC: 0185-0034-51
Package Description: 150 TABLET in 1 BOTTLE (0185-0034-51)

NDC Information of tizanidine hydrochloride

NDC Code 0185-0034-51
Proprietary Name tizanidine hydrochloride
Package Description 150 TABLET in 1 BOTTLE (0185-0034-51)
Product NDC 0185-0034
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 Eon Labs, 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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