Clopidogrel Bisulfate

Product NDC
71335-0752
11-digit product format
713350752
Labeler code
71335
Product ID
71335-0752_ba1479ef-ff82-4d64-af2c-10425fcbd5ab
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clopidogrel Bisulfate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA090494
Marketing category
ANDA
Marketing start
2012-05-18
Marketing end
0000-00-00
Substance
CLOPIDOGREL BISULFATE
Active strength
75 mg/1
Pharmacologic classes
Cytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-0752-1EA - Each71335-07520f1d16f5-6ed1-4fc4-8ff8-fb5d364a94d012022-10-06
71335-0752-2EA - Each71335-0752daeb0500-f76d-436c-b80a-d10d9cf0cf0e12018-08-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0752-17133507520190 TABLET, FILM COATED in 1 BOTTLE (71335-0752-1) 2016-11-290000-00-00NoNoCurrent
71335-0752-27133507520230 TABLET, FILM COATED in 1 BOTTLE (71335-0752-2) 2016-11-290000-00-00NoNoCurrent
71335-0752-37133507520360 TABLET, FILM COATED in 1 BOTTLE (71335-0752-3) 2016-11-290000-00-00NoNoCurrent
71335-0752-47133507520420 TABLET, FILM COATED in 1 BOTTLE (71335-0752-4) 2016-11-290000-00-00NoNoCurrent
71335-0752-57133507520510 TABLET, FILM COATED in 1 BOTTLE (71335-0752-5) 2022-01-270000-00-00NoNoCurrent