Lisinopril

Product NDC
53808-0703
11-digit product format
538080703
Labeler code
53808
Product ID
53808-0703_27c6283e-54e1-4ae0-a07a-dc71d92a6de2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LISINOPRIL
Dosage form
TABLET
Route
ORAL
Labeler
State of Florida DOH Central Pharmacy
Application
ANDA076059
Marketing category
ANDA
Marketing start
2009-07-01
Marketing end
0000-00-00
Substance
LISINOPRIL
Active strength
20 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
E7199S1YWRLISINOPRIL83915-83-7LISINOPRIL

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ONCE-DAILY Lisinopril Tablets USP Rx onlyState of Florida DOH Central Pharmacy2010-03-08HUMAN PRESCRIPTION DRUG LABEL2