Home > National Drug Code (NDC) > Ticlopidine Hydrochloride

Ticlopidine Hydrochloride - 0185-0115-30 - (Ticlopidine Hydrochloride)

Alphabetical Index


Drug Information of Ticlopidine Hydrochloride

Product NDC: 0185-0115
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: 0185-0115
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075326
Marketing Category: ANDA
Start Marketing Date: 19990820

Package Information of Ticlopidine Hydrochloride

Package NDC: 0185-0115-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0185-0115-30)

NDC Information of Ticlopidine Hydrochloride

NDC Code 0185-0115-30
Proprietary Name Ticlopidine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0185-0115-30)
Product NDC 0185-0115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ticlopidine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19990820
Marketing Category Name ANDA
Labeler Name Eon Labs, 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


General Information