Clopidogrel Bisulfate

Product NDC
55154-5388
11-digit product format
551545388
Labeler code
55154
Product ID
55154-5388_6614895e-08b2-49ba-a1af-53024cca684d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clopidogrel
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Cardinal Health
Application
ANDA077665
Marketing category
ANDA
Marketing start
2012-06-08
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55154-5388-0EA - Each55154-5388bea37c2d-18f1-4bc4-aa5b-710c9e0af5b712019-05-02