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TIZANIDINE HYDROCHLORIDE - 68387-130-90 - (TIZANIDINE HYDROCHLORIDE)

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Drug Information of TIZANIDINE HYDROCHLORIDE

Product NDC: 68387-130
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: 68387-130
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076347
Marketing Category: ANDA
Start Marketing Date: 20050601

Package Information of TIZANIDINE HYDROCHLORIDE

Package NDC: 68387-130-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (68387-130-90)

NDC Information of TIZANIDINE HYDROCHLORIDE

NDC Code 68387-130-90
Proprietary Name TIZANIDINE HYDROCHLORIDE
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (68387-130-90)
Product NDC 68387-130
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TIZANIDINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050601
Marketing Category Name ANDA
Labeler Name Keltman 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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