Effient

Product NDC
0002-5123
11-digit product format
000025123
Labeler code
0002
Product ID
0002-5123_6d9c1bbc-8783-4a3d-a487-1868b3c37b14
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prasugrel hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Eli Lilly and Company
Application
NDA022307
Marketing category
NDA
Marketing start
2009-07-10
Marketing end
2022-03-31
Substance
PRASUGREL HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0002-5123-01EA - Each0002-5123e6dee7f1-a5b1-4783-9c2d-af547b92e75212013-02-13
0002-5123-30EA - Each0002-5123b988377d-17a5-416a-b2b9-b497d18a113612012-07-24
0002-5123-77EA - Each0002-5123a7efd4ec-7fa7-4e9f-82d8-4711c588c26a12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0002-5123-300000251233030 TABLET, FILM COATED in 1 BOTTLE (0002-5123-30) 2012-03-010000-00-00NoNoCurrent
0002-5123-770000251237790 BLISTER PACK in 1 CARTON (0002-5123-77) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0002-5123-01) 90 blister pack2012-03-010000-00-00NoNoCurrent