Lisinopril

Product NDC
55289-917
11-digit product format
552890917
Labeler code
55289
Product ID
55289-917_7b2d3424-4a38-565f-e053-2a91aa0a297b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA076063
Marketing category
ANDA
Marketing start
2002-07-01
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
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
55289-917-30EA - Each55289-9174f1000de-27ff-45fa-bc43-4dc748b7cadc12013-09-04
55289-917-90EA - Each55289-9175f176247-c1e2-449c-8cec-af30da3df87a12013-09-04