lisinopril

Product NDC
66267-583
11-digit product format
662670583
Labeler code
66267
Product ID
66267-583_9cbcf79b-1b86-24ad-e053-2995a90a5eac
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA075994
Marketing category
ANDA
Marketing start
2015-06-09
Marketing end
0000-00-00
Substance
LISINOPRIL
Active strength
40 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-583-30EA - Each66267-5833144c79f-142a-415d-9855-d7da523e87f312017-03-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66267-583-306626705833030 TABLET in 1 BOTTLE (66267-583-30) 30 tablet2016-12-230000-00-00NoNoCurrent
66267-583-606626705836060 TABLET in 1 BOTTLE (66267-583-60) 60 tablet2016-12-230000-00-00NoNoCurrent
66267-583-906626705839090 TABLET in 1 BOTTLE (66267-583-90) 90 tablet2016-12-230000-00-00NoNoCurrent