NDC Code(s) : 55154-4564-9
Packager : Cardinal Health

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Metoprolol TartrateMetoprolol tartrate TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:55154-4564(NDC:57664-477)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
METOPROLOL TARTRATE(UNII: W5S57Y3A5L)
(METOPROLOL - UNII:GEB06NHM23) 		METOPROLOL TARTRATE50 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
HYPROMELLOSES(UNII: 3NXW29V3WO)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE(UNII: OP1R32D61U)
POLYETHYLENE GLYCOLS(UNII: 3WJQ0SDW1A)
POLYSORBATE 20(UNII: 7T1F30V5YH)
POVIDONES(UNII: FZ989GH94E)
SODIUM STARCH GLYCOLATE TYPE A POTATO(UNII: 5856J3G2A2)
TALC(UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
Product Characteristics
Color WHITE (WHITE) Score 2 pieces
Shape ROUND Size 8 mm
Flavor Imprint Code 477
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:55154-4564-930 in 1 BLISTER PACK
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074644 07/01/1997

PRINCIPAL DISPLAY PANEL

Metoprolol Tartrate Tablets, USP

50 mg

30 Tablets

Lidding Label