LISINOPRIL

Product NDC
71610-731
11-digit product format
716100731
Labeler code
71610
Product ID
71610-731_471f70ee-df85-0cf8-e063-6294a90ad68f
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
10 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
71610-731-157161007311515 TABLET in 1 BOTTLE (71610-731-15) 15 tablet2023-09-06NoNoHistorical
71610-731-307161007313030 TABLET in 1 BOTTLE (71610-731-30) 30 tablet2023-09-06NoNoHistorical
71610-731-457161007314545 TABLET in 1 BOTTLE (71610-731-45) 45 tablet2023-09-06NoNoHistorical
71610-731-607161007316090 TABLET in 1 BOTTLE (71610-731-60) 90 tablet2023-09-06NoNoHistorical
71610-731-8071610073180180 TABLET in 1 BOTTLE (71610-731-80) 180 tablet2023-09-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LISINOPRILAphena Pharma Solutions - Tennessee, LLC2025-12-29HUMAN PRESCRIPTION DRUG LABEL4