Effient

Product NDC
65597-602
11-digit product format
655970602
Labeler code
65597
Product ID
65597-602_e1bbf5b8-ba73-4152-9f77-9e73d6699c16
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prasugrel Hydrochloride
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Daiichi Sankyo, Inc.
Application
NDA022307
Marketing category
NDA
Marketing start
2009-07-10
Marketing end
2023-12-31
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
65597-602-30EA - Each65597-602c553fdbe-7a8a-4a9c-a455-d52401ae843812021-08-05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
65597-602-306559706023030 TABLET, COATED in 1 BOTTLE (65597-602-30) 2021-07-010000-00-00NoNoCurrent