LISINOPRIL

Product NDC
71610-766
11-digit product format
716100766
Labeler code
71610
Product ID
71610-766_0f42d62b-5179-4b4e-ad6a-b718ce03de19
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LISINOPRIL
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA076102
Marketing category
ANDA
Marketing start
2023-04-07
Substance
LISINOPRIL
Active strength
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
71610-766-307161007663030 TABLET in 1 BOTTLE (71610-766-30) 30 tablet2024-01-03NoNoHistorical
71610-766-537161007665360 TABLET in 1 BOTTLE (71610-766-53) 60 tablet2024-01-03NoNoHistorical
71610-766-607161007666090 TABLET in 1 BOTTLE (71610-766-60) 90 tablet2024-01-03NoNoHistorical
71610-766-8071610076680180 TABLET in 1 BOTTLE (71610-766-80) 180 tablet2024-01-03NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LISINOPRILAphena Pharma Solutions - Tennessee, LLC2024-01-04HUMAN PRESCRIPTION DRUG LABEL1