Lisinopril

Product NDC
57237-055
11-digit product format
572370055
Labeler code
57237
Product ID
57237-055_dc0a5a29-63b0-44f6-ad5b-e39e7634b5b4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Citron Pharma LLC
Application
ANDA077622
Marketing category
ANDA
Marketing start
2006-02-22
Marketing end
0000-00-00
Substance
LISINOPRIL
Active strength
20 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
57237-055-00EA - Each57237-055701e14d9-2fb2-4f7a-803d-baeb812eb34412014-04-03
57237-055-99EA - Each57237-055d4f518ca-6775-46d5-8a7e-e5db3855e96012014-04-03