NDC Code(s) : 50090-1273-0, 50090-1273-1, 50090-1273-2, 50090-1273-3
Packager : A-S Medication Solutions

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:50090-1273(NDC:57664-506)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
METOPROLOL TARTRATE(UNII: W5S57Y3A5L)
(METOPROLOL - UNII:GEB06NHM23) 		METOPROLOL TARTRATE25 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
HYPROMELLOSE, UNSPECIFIED(UNII: 3NXW29V3WO)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED(UNII: 3WJQ0SDW1A)
POLYSORBATE 20(UNII: 7T1F30V5YH)
POVIDONE, UNSPECIFIED(UNII: FZ989GH94E)
SODIUM STARCH GLYCOLATE TYPE A POTATO(UNII: 5856J3G2A2)
TALC(UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
Product Characteristics
Color WHITE (WHITE) Score no score
Shape ROUND (circular) Size 5 mm
Flavor Imprint Code 1
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:50090-1273-0180 in 1 BOTTLE Type 0: Not a Combination Product29/06/2015
2NDC:50090-1273-160 in 1 BOTTLE Type 0: Not a Combination Product29/06/2015
3NDC:50090-1273-290 in 1 BOTTLE Type 0: Not a Combination Product29/06/2015
4NDC:50090-1273-330 in 1 BOTTLE Type 0: Not a Combination Product29/06/2015
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076670 06/29/2015 05/31/2017

PRINCIPAL DISPLAY PANEL

Label Image