Lisinopril

Product NDC
42708-095
11-digit product format
427080095
Labeler code
42708
Product ID
42708-095_9f05cf28-0e05-4e86-a495-4af18f52352d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
QPharma Inc
Application
ANDA075743
Marketing category
ANDA
Marketing start
2002-07-01
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
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42708-095-302021-03-12C16284748780-1ba0f9c33-435c-a910-e053-dadaa90a0b85d054e4ba-ff91-481b-bb77-320d38109c62
42708-095-302021-01-29C16284748780-1ba0f9c33-435c-a910-e053-dadaa90a0b85d054e4ba-ff91-481b-bb77-320d38109c62