LISINOPRIL

Product NDC
63187-534
11-digit product format
631870534
Labeler code
63187
Product ID
63187-534_fbdbc52b-3eb9-4ec8-98d1-ab04e553fdc1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA076180
Marketing category
ANDA
Marketing start
2011-11-01
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
63187-534-306318705343030 TABLET in 1 BOTTLE (63187-534-30) 30 tablet2018-12-01NoNoHistorical
63187-534-606318705346060 TABLET in 1 BOTTLE (63187-534-60) 60 tablet2018-12-01NoNoHistorical
63187-534-906318705349090 TABLET in 1 BOTTLE (63187-534-90) 90 tablet2018-12-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LISINOPRILProficient Rx LP2023-05-01HUMAN PRESCRIPTION DRUG LABEL4