Lisinopril

Product NDC
71610-741
11-digit product format
716100741
Labeler code
71610
Product ID
71610-741_9f5db76f-349d-4856-b7d9-ded1ab8ca656
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA075743
Marketing category
ANDA
Marketing start
2017-08-30
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
71610-741-307161007413030 TABLET in 1 BOTTLE (71610-741-30) 30 tablet2023-10-03NoNoHistorical
71610-741-457161007414545 TABLET in 1 BOTTLE (71610-741-45) 45 tablet2023-10-03NoNoHistorical
71610-741-537161007415360 TABLET in 1 BOTTLE (71610-741-53) 60 tablet2023-10-03NoNoHistorical
71610-741-607161007416090 TABLET in 1 BOTTLE (71610-741-60) 90 tablet2023-10-03NoNoHistorical
71610-741-7071610074170120 TABLET in 1 BOTTLE (71610-741-70) 120 tablet2023-10-03NoNoHistorical
71610-741-7571610074175150 TABLET in 1 BOTTLE (71610-741-75) 150 tablet2023-10-03NoNoHistorical
71610-741-8071610074180180 TABLET in 1 BOTTLE (71610-741-80) 180 tablet2023-10-03NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LisinoprilAphena Pharma Solutions - Tennessee, LLC2023-10-04HUMAN PRESCRIPTION DRUG LABEL1