NDC Code(s) : 63629-3475-1
Packager : Bryant Ranch Prepack

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

TOPROL Metoprolol succinate TABLET, EXTENDED RELEASE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63629-3475(NDC:0186-1094)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
METOPROLOL SUCCINATE(UNII: TH25PD4CCB)
(METOPROLOL - UNII:GEB06NHM23) 		METOPROLOL200 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM STEARYL FUMARATE(UNII: 7CV7WJK4UI)
POLYETHYLENE GLYCOL 6000(UNII: 30IQX730WE)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
PARAFFIN(UNII: I9O0E3H2ZE)
HYPROMELLOSE, UNSPECIFIED(UNII: 3NXW29V3WO)
Product Characteristics
Color WHITE Score 2 pieces
Shape OVAL (biconvex) Size 17 mm
Flavor Imprint Code A;my
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:63629-3475-11 in 1 BOTTLE Type 0: Not a Combination Product02/01/1992
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA019962 02/01/1992

PRINCIPAL DISPLAY PANEL

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