Integrilin

Product NDC
0085-1136
11-digit product format
000851136
Labeler code
0085
Product ID
0085-1136_18b14fcd-6c25-4112-876f-1dd811c95ed4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Eptifibatide
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Merck Sharp & Dohme Corp.
Application
NDA020718
Marketing category
NDA
Marketing start
1998-05-18
Marketing end
0000-00-00
Substance
EPTIFIBATIDE
Active strength
1 mg/mL
Pharmacologic classes
Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
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
0085-1136-01ML - Milliliter0085-1136923fbb58-a6ff-4628-9354-0fe6c0f1eb6012012-07-24
0085-1136-02ML - Milliliter0085-1136e0bc8f86-9461-4199-8627-509a015074e712014-09-03
0085-1136-03ML - Milliliter0085-1136492fc689-4aae-4c99-b8d7-beacb08a258312015-06-09

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0085-1136-01000851136011 VIAL, SINGLE-USE in 1 CARTON (0085-1136-01) > 100 mL in 1 VIAL, SINGLE-USE1998-05-180000-00-00NoNoCurrent