NDC 71335-0080 – Clopidogrel

Clopidogrel Bisulfate 75 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0080

Product details

Brand name
Clopidogrel
Generic name
Clopidogrel Bisulfate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090540
Marketed since
May 17, 2012
Listing expires
December 31, 2026
Pharmacologic class
P2Y12 Platelet Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Clopidogrel →

Package NDC codes (5)

Package NDCDescriptionSince
71335-0080-190 TABLET, FILM COATED in 1 BOTTLE (71335-0080-1)Apr 21, 2023
71335-0080-230 TABLET, FILM COATED in 1 BOTTLE (71335-0080-2)May 2, 2023
71335-0080-360 TABLET, FILM COATED in 1 BOTTLE (71335-0080-3)May 29, 2024
71335-0080-420 TABLET, FILM COATED in 1 BOTTLE (71335-0080-4)May 29, 2024
71335-0080-510 TABLET, FILM COATED in 1 BOTTLE (71335-0080-5)May 29, 2024

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