NDC Code(s) : 52125-213-02
Packager : REMEDYREPACK INC.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

LisinoprilLISINOPRIL TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52125-213(NDC:0172-3758)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LISINOPRIL(UNII: E7199S1YWR)
(LISINOPRIL ANHYDROUS - UNII:7Q3P4BS2FD) 		LISINOPRIL5 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS DIBASIC CALCIUM PHOSPHATE(UNII: L11K75P92J)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MANNITOL(UNII: 3OWL53L36A)
STARCH, CORN(UNII: O8232NY3SJ)
TALC(UNII: 7SEV7J4R1U)
Product Characteristics
Color white Score 2 pieces
Shape SQUARE (TABLET) Size 6 mm
Flavor Imprint Code 3758
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:52125-213-0230 in 1 BLISTER PACK Type 0: Not a Combination Product20/08/2012
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075752 08/20/2012 04/04/2014

PRINCIPAL DISPLAY PANEL

DRUG: Lisinopril

GENERIC: LISINOPRIL

DOSAGE: TABLET

ADMINSTRATION: ORAL

NDC: 52125-213-02

STRENGTH:5 mg

COLOR: white

SHAPE: SQUARE

SCORE: Two even pieces

SIZE: 6 mm

IMPRINT: 30

QTY: 30

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