NDC Code(s) : 52125-165-02
Packager : REMEDYREPACK INC.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

lisinopril lisinopril TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52125-165(NDC:0185-0102)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISINOPRIL(UNII: E7199S1YWR)
(LISINOPRIL ANHYDROUS - UNII:7Q3P4BS2FD) 		LISINOPRIL20 mg
Inactive Ingredients
Ingredient Name Strength
CALCIUM PHOSPHATE(UNII: 97Z1WI3NDX)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MANNITOL(UNII: 3OWL53L36A)
FERRIC OXIDE RED(UNII: 1K09F3G675)
STARCH, CORN(UNII: O8232NY3SJ)
FERRIC OXIDE YELLOW(UNII: EX438O2MRT)
Product Characteristics
Color orange Score 2 pieces
Shape OVAL (TABLET) Size 10 mm
Flavor Imprint Code E102
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:52125-165-0230 in 1 BLISTER PACK
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075994 03/20/2013

PRINCIPAL DISPLAY PANEL

DRUG: lisinopril
GENERIC: lisinopril
DOSAGE: TABLET
ADMINSTRATION: ORAL
NDC: 52125-165-02
STRENGTH:20 mg
COLOR: orange
SHAPE: OVAL
SCORE: Two even pieces
SIZE: 10 mm
IMPRINT: 30
QTY: 30

/xml/210d7643-7e07-4421-a013-6df20923056f/MM2.jpg/xml/210d7643-7e07-4421-a013-6df20923056f/MM2.jpg