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Ticlopidine Hydrochloride - 57664-327-06 - (Ticlopidine Hydrochloride)

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Drug Information of Ticlopidine Hydrochloride

Product NDC: 57664-327
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: 57664-327
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075526
Marketing Category: ANDA
Start Marketing Date: 20020926

Package Information of Ticlopidine Hydrochloride

Package NDC: 57664-327-06
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (57664-327-06)

NDC Information of Ticlopidine Hydrochloride

NDC Code 57664-327-06
Proprietary Name Ticlopidine Hydrochloride
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (57664-327-06)
Product NDC 57664-327
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ticlopidine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020926
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd.
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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