LISINOPRIL

Product NDC
76420-343
11-digit product format
764200343
Labeler code
76420
Product ID
76420-343_342374a0-645e-e49e-e063-6394a90a2498
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA076164
Marketing category
ANDA
Marketing start
2011-11-01
Substance
LISINOPRIL
Active strength
20 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
76420-343-00764200343001000 TABLET in 1 BOTTLE (76420-343-00) 1000 tablet2025-05-02NoNoHistorical
76420-343-0176420034301100 TABLET in 1 BOTTLE (76420-343-01) 100 tablet2025-05-02NoNoHistorical
76420-343-307642003433030 TABLET in 1 BOTTLE (76420-343-30) 30 tablet2025-05-02NoNoHistorical
76420-343-607642003436060 TABLET in 1 BOTTLE (76420-343-60) 60 tablet2025-05-02NoNoHistorical
76420-343-907642003439090 TABLET in 1 BOTTLE (76420-343-90) 90 tablet2025-05-02NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LISINOPRILAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2025-05-02HUMAN PRESCRIPTION DRUG LABEL1