Lisinopril

Product NDC
21695-330
11-digit product format
216950330
Labeler code
21695
Product ID
21695-330_612dfaac-f178-4880-b38d-2456478d738a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Rebel Distributors Corp
Application
ANDA076059
Marketing category
ANDA
Marketing start
2002-07-01
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 Revised: September 2008 Rx only 2000258-02Rebel Distributors Corp2010-10-01HUMAN PRESCRIPTION DRUG LABEL2