Lisinopril

Product NDC
50436-4000
11-digit product format
504364000
Labeler code
50436
Product ID
50436-4000_a36c3511-0056-41e7-b6de-2950f9c1d86f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Unit Dose Services
Application
ANDA076063
Marketing category
ANDA
Marketing start
2002-07-01
Marketing end
0000-00-00
Substance
LISINOPRIL
Active strength
10 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50436-4000-3EA - Each50436-4000bfc84251-70f2-4755-932f-6ddca0dec95e12016-10-06