Clopidogrel

Product NDC

70518-0750

11-digit product format

705180750

Labeler code

70518

Product ID

70518-0750_8e7b962e-d420-1685-e053-2995a90a8ccc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Clopidogrel bisulphate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA202925

Marketing category

ANDA

Marketing start

2017-09-27

Marketing end

0000-00-00

Substance

CLOPIDOGREL BISULFATE

Active strength

75 mg/1

Pharmacologic classes

Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA],Cytochrome P450 2C8 Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record