Lisinopril

Product NDC
71610-638
11-digit product format
716100638
Labeler code
71610
Product ID
71610-638_d7a97460-5f05-45fe-8943-23c7c8f1deef
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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
71610-638-157161006381515 TABLET in 1 BOTTLE (71610-638-15) 15 tablet2022-03-09NoNoHistorical
71610-638-307161006383030 TABLET in 1 BOTTLE (71610-638-30) 30 tablet2022-03-09NoNoHistorical
71610-638-457161006384545 TABLET in 1 BOTTLE (71610-638-45) 45 tablet2022-03-09NoNoHistorical
71610-638-607161006386090 TABLET in 1 BOTTLE (71610-638-60) 90 tablet2022-03-09NoNoHistorical
71610-638-8071610063880180 TABLET in 1 BOTTLE (71610-638-80) 180 tablet2022-03-09NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LisinoprilAphena Pharma Solutions - Tennessee, LLC2022-03-10HUMAN PRESCRIPTION DRUG LABEL1