Clopidogrel

Product NDC
64679-315
11-digit product format
646790315
Labeler code
64679
Product ID
64679-315_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
2012-11-20
Marketing end
0000-00-00
Substance
CLOPIDOGREL BISULFATE
Active strength
300 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
64679-315-01EA - Each64679-315e3a82f82-3a61-4561-a694-dcfc6d43ace412013-02-13
64679-315-02EA - Each64679-315e6554a81-8e96-4465-b63f-9a603133491012013-02-13