Clopidogrel

Product NDC
64679-314
11-digit product format
646790314
Labeler code
64679
Product ID
64679-314_a7370f50-bd1e-4ce4-8cd0-4ba6c0d6bfe4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clopidogrel
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Wockhardt USA LLC.
Application
ANDA202266
Marketing category
ANDA
Marketing start
2012-08-14
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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
64679-314-00EA - Each64679-3143ee252b1-ad39-4977-abca-80b51cbefd9a12013-02-13
64679-314-01EA - Each64679-31490302660-7f3d-465c-b5ab-8ce3094d67be12013-02-13
64679-314-02EA - Each64679-314cacc62f6-4a14-4363-bacf-3800525b274212013-02-13
64679-314-03EA - Each64679-314e740d3c7-8844-475a-8de0-e345deae284b12013-03-03