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Tizanidine Hydrochloride - 68084-013-01 - (Tizanidine Hydrochloride)

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Drug Information of Tizanidine Hydrochloride

Product NDC: 68084-013
Proprietary Name: Tizanidine Hydrochloride
Non Proprietary Name: Tizanidine Hydrochloride
Active Ingredient(s): 4    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: 68084-013
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076286
Marketing Category: ANDA
Start Marketing Date: 20130708

Package Information of Tizanidine Hydrochloride

Package NDC: 68084-013-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-013-01) > 10 TABLET in 1 BLISTER PACK (68084-013-11)

NDC Information of Tizanidine Hydrochloride

NDC Code 68084-013-01
Proprietary Name Tizanidine Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-013-01) > 10 TABLET in 1 BLISTER PACK (68084-013-11)
Product NDC 68084-013
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tizanidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130708
Marketing Category Name ANDA
Labeler Name American Health Packaging
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 Hydrochloride


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