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Ticlopidine Hydrochloride - 0093-0154-01 - (Ticlopidine Hydrochloride)

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Drug Information of Ticlopidine Hydrochloride

Product NDC: 0093-0154
Proprietary Name: Ticlopidine Hydrochloride
Non Proprietary Name: Ticlopidine Hydrochloride
Active Ingredient(s): 250    mg/1 & nbsp;   Ticlopidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ticlopidine Hydrochloride

Product NDC: 0093-0154
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075149
Marketing Category: ANDA
Start Marketing Date: 19990907

Package Information of Ticlopidine Hydrochloride

Package NDC: 0093-0154-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-0154-01)

NDC Information of Ticlopidine Hydrochloride

NDC Code 0093-0154-01
Proprietary Name Ticlopidine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-0154-01)
Product NDC 0093-0154
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ticlopidine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19990907
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name TICLOPIDINE HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]

Complete Information of Ticlopidine Hydrochloride


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