Ticlopidine Hydrochloride

Product NDC

57664-327

11-digit product format

576640327

Labeler code

57664

Product ID

57664-327_aa3b8a6e-c60c-47e3-8ccf-54d73c7e42aa

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ticlopidine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Caraco Pharmaceutical Laboratories, Ltd.

Application

ANDA075526

Marketing category

ANDA

Marketing start

2002-09-26

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record