Lisinopril

Product NDC
50090-5120
11-digit product format
500905120
Labeler code
50090
Product ID
50090-5120_2a8f2e4b-c3d2-45cf-9e79-58200e801223
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077321
Marketing category
ANDA
Marketing start
2017-05-12
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
50090-5120-05009051200030 TABLET in 1 BOTTLE (50090-5120-0) 30 tablet2020-08-05NoNoHistorical
50090-5120-150090512001100 TABLET in 1 BOTTLE (50090-5120-1) 100 tablet2020-08-05NoNoHistorical
50090-5120-35009051200360 TABLET in 1 BOTTLE (50090-5120-3) 60 tablet2020-08-05NoNoHistorical
50090-5120-450090512004200 TABLET in 1 BOTTLE (50090-5120-4) 200 tablet2020-08-05NoNoHistorical
50090-5120-55009051200590 TABLET in 1 BOTTLE (50090-5120-5) 90 tablet2020-08-05NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LisinoprilA-S Medication Solutions2023-03-27HUMAN PRESCRIPTION DRUG LABEL48