Ticlopidine Hydrochloride

Product NDC

0185-0115

11-digit product format

001850115

Labeler code

0185

Product ID

0185-0115_69bb6c03-a786-4ced-9d02-ee541657f376

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ticlopidine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Eon Labs, Inc.

Application

ANDA075326

Marketing category

ANDA

Marketing start

1999-08-20

Marketing end

0000-00-00

Substance

TICLOPIDINE HYDROCHLORIDE

Active strength

250 mg/1

Pharmacologic classes

Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record