Lisinopril

Product NDC
0615-7643
11-digit product format
006157643
Labeler code
0615
Product ID
0615-7643_35e2befc-faf9-486b-97d3-71f98e7e6982
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA078402
Marketing category
ANDA
Marketing start
2007-04-19
Marketing end
0000-00-00
Substance
LISINOPRIL
Active strength
30 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-7643-392022-11-09C16284748780-19d75b9d1-0b97-f424-e053-dadaa90a57cee9385674-c074-4854-9b5c-655846cd8e09
0615-7643-392020-01-31C16284748780-19d75b9d1-0b97-f424-e053-dadaa90a57cee9385674-c074-4854-9b5c-655846cd8e09