Metoprolol Tartrate (Page 5 of 5)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL — 25 mg (60 Tablet Bottle)

Metoprolol Tartrate 25mg Tablets
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PACKAGE LABEL-PRINCIPAL DISPLAY PANEL — 50 mg (60 Tablet Bottle)

Metoprolol Tartrate 50mg Tablets
(click image for full-size original)
METOPROLOL TARTRATE metoprolol tartrate tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70882-132(NDC:65862-062)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
METOPROLOL TARTRATE (METOPROLOL) METOPROLOL TARTRATE 25 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
SILICON DIOXIDE
SODIUM LAURYL SULFATE
TALC
MAGNESIUM STEARATE
HYPROMELLOSE 2910 (6 MPA.S)
TITANIUM DIOXIDE
POLYETHYLENE GLYCOL 400
POLYSORBATE 80
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 7mm
Flavor Imprint Code C;73
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70882-132-60 60 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077739 09/11/2007
METOPROLOL TARTRATE metoprolol tartrate tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70882-133(NDC:65862-063)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
METOPROLOL TARTRATE (METOPROLOL) METOPROLOL TARTRATE 50 mg
Inactive Ingredients
Ingredient Name Strength
CELLULOSE, MICROCRYSTALLINE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
SILICON DIOXIDE
SODIUM LAURYL SULFATE
TALC
MAGNESIUM STEARATE
HYPROMELLOSE 2910 (6 MPA.S)
TITANIUM DIOXIDE
POLYETHYLENE GLYCOL 400
POLYSORBATE 80
D&C RED NO. 30
Product Characteristics
Color PINK Score 2 pieces
Shape ROUND Size 8mm
Flavor Imprint Code C;74
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70882-133-60 60 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077739 09/11/2007
Labeler — Cambridge Therapeutics Technologies, LLC (080072003)

Revised: 10/2017 Cambridge Therapeutics Technologies, LLC

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