LISINOPRIL

Product NDC
71335-0075
11-digit product format
713350075
Labeler code
71335
Product ID
71335-0075_e9965b5f-6613-452f-b7e9-4b58a51e8c76
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
40 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
71335-0075-17133500750130 TABLET in 1 BOTTLE (71335-0075-1) 30 tablet2022-03-15NoNoHistorical
71335-0075-271335007502100 TABLET in 1 BOTTLE (71335-0075-2) 100 tablet2022-03-15NoNoHistorical
71335-0075-37133500750390 TABLET in 1 BOTTLE (71335-0075-3) 90 tablet2022-03-15NoNoHistorical
71335-0075-47133500750460 TABLET in 1 BOTTLE (71335-0075-4) 60 tablet2022-03-15NoNoHistorical
71335-0075-571335007505180 TABLET in 1 BOTTLE (71335-0075-5) 180 tablet2022-03-15NoNoHistorical
71335-0075-67133500750614 TABLET in 1 BOTTLE (71335-0075-6) 14 tablet2022-03-15NoNoHistorical
71335-0075-771335007507120 TABLET in 1 BOTTLE (71335-0075-7) 120 tablet2022-03-15NoNoHistorical
71335-0075-87133500750810 TABLET in 1 BOTTLE (71335-0075-8) 10 tablet2022-03-15NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LISINOPRILBryant Ranch Prepack2024-08-26HUMAN PRESCRIPTION DRUG LABEL102