NDC 55111-671 – Clopidogrel bisulfate

Clopidogrel Bisulfate 300 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 2 recalls

Product NDC55111-671

Product details

Brand name
Clopidogrel bisulfate
Generic name
Clopidogrel bisulfate
Labeler
Dr.Reddy's Laboratories Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091023
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 bisulfate →

Package NDC codes (8)

Package NDCDescriptionSince
55111-671-01100 TABLET, FILM COATED in 1 BOTTLE (55111-671-01)May 17, 2012
55111-671-05500 TABLET, FILM COATED in 1 BOTTLE (55111-671-05)May 17, 2012
55111-671-3030 TABLET, FILM COATED in 1 BOTTLE (55111-671-30)May 17, 2012
55111-671-315 BLISTER PACK in 1 CARTON (55111-671-31) / 6 TABLET, FILM COATED in 1 BLISTER PACK (55111-671-06)May 17, 2012
55111-671-481 BLISTER PACK in 1 CARTON (55111-671-48) / 4 TABLET, FILM COATED in 1 BLISTER PACKMay 17, 2012
55111-671-7810 BLISTER PACK in 1 CARTON (55111-671-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-671-79)May 17, 2012
55111-671-813 BLISTER PACK in 1 CARTON (55111-671-81) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-671-79)May 17, 2012
55111-671-9090 TABLET, FILM COATED in 1 BOTTLE (55111-671-90)May 17, 2012

Recalls mentioning this NDC

Other Clopidogrel bisulfate products