Clopidogrel bisulfate

Product NDC

68071-4057

11-digit product format

680714057

Labeler code

68071

Product ID

68071-4057_56f72c95-63c7-30f6-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Clopidogrel bisulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA204165

Marketing category

ANDA

Marketing start

2017-05-05

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

2019-12-31

Current FDA listing

Historical FDA.report record