LISINOPRIL

Product NDC
71335-0498
11-digit product format
713350498
Labeler code
71335
Product ID
71335-0498_63976f80-e102-4fdb-8617-572c13a57077
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076164
Marketing category
ANDA
Marketing start
2011-11-01
Substance
LISINOPRIL
Active strength
2.5 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
E7199S1YWRLISINOPRIL83915-83-7LISINOPRIL

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-0498-17133504980130 TABLET in 1 BOTTLE (71335-0498-1) 30 tablet2018-09-25NoNoHistorical
71335-0498-27133504980290 TABLET in 1 BOTTLE (71335-0498-2) 90 tablet2018-02-12NoNoHistorical
71335-0498-37133504980360 TABLET in 1 BOTTLE (71335-0498-3) 60 tablet2024-10-08NoNoHistorical
71335-0498-47133504980410 TABLET in 1 BOTTLE (71335-0498-4) 10 tablet2024-10-08NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LISINOPRILBryant Ranch Prepack2024-10-08HUMAN PRESCRIPTION DRUG LABEL102