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TIZANIDINE HYDROCHLORIDE - 21695-126-78 - (TIZANIDINE HYDROCHLORIDE)

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Drug Information of TIZANIDINE HYDROCHLORIDE

Product NDC: 21695-126
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: 21695-126
Labeler Name: Rebel Distributors
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076347
Marketing Category: ANDA
Start Marketing Date: 20070206

Package Information of TIZANIDINE HYDROCHLORIDE

Package NDC: 21695-126-78
Package Description: 180 TABLET in 1 BOTTLE (21695-126-78)

NDC Information of TIZANIDINE HYDROCHLORIDE

NDC Code 21695-126-78
Proprietary Name TIZANIDINE HYDROCHLORIDE
Package Description 180 TABLET in 1 BOTTLE (21695-126-78)
Product NDC 21695-126
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TIZANIDINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070206
Marketing Category Name ANDA
Labeler Name Rebel Distributors
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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