Effient

Product NDC
0002-5121
11-digit product format
000025121
Labeler code
0002
Product ID
0002-5121_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
2022-02-28
Substance
PRASUGREL HYDROCHLORIDE
Active strength
5 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
0002-5121-01EA - Each0002-5121ba5e3d09-8994-46ef-90ce-9f5ba3cfab1612013-02-13
0002-5121-30EA - Each0002-51217b79a868-2067-4846-8b1a-4ebaf933777d12012-07-24
0002-5121-52EA - Each0002-5121bea1fb24-b871-48e8-aaaa-bd78a817594d12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0002-5121-300000251213030 TABLET, FILM COATED in 1 BOTTLE (0002-5121-30) 2012-03-010000-00-00NoNoCurrent
0002-5121-520000251215224 BLISTER PACK in 1 CARTON (0002-5121-52) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0002-5121-01) 24 blister pack2012-03-010000-00-00NoNoCurrent