Lisinopril

Product NDC
71610-624
11-digit product format
716100624
Labeler code
71610
Product ID
71610-624_6224d557-1df2-46fb-bebd-eb8bdf81c897
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA077321
Marketing category
ANDA
Marketing start
2021-06-01
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
71610-624-457161006244545 TABLET in 1 BOTTLE (71610-624-45) 45 tablet2021-12-06NoNoHistorical
71610-624-607161006246090 TABLET in 1 BOTTLE (71610-624-60) 90 tablet2021-12-06NoNoHistorical
71610-624-8071610062480180 TABLET in 1 BOTTLE (71610-624-80) 180 tablet2022-02-07NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LisinoprilAphena Pharma Solutions - Tennessee, LLC2022-03-03HUMAN PRESCRIPTION DRUG LABEL2