SOTALOL (Page 8 of 8)

Manufactured by
MUTUAL PHARMACEUTICAL COMPANY, INC.Philadelphia, PA 19124 USA

Rev: October 2003Ch

SOTALOL sotalol tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53489-503
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
sotalol (sotalol) sotalol 80 mg
Inactive Ingredients
Ingredient Name Strength
Anhydrous lactose
colloidal silicon dioxide
corn starch
magnesium stearate
microcrystalline cellulose
pregelatinized starch
sodium starch glycolate
stearic acid
Product Characteristics
Color WHITE Score 2 pieces
Shape OVAL Size 11mm
Flavor Imprint Code MP;518
Contains
Coating false Symbol false
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53489-503-07 30 TABLET (30 TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:53489-503-06 60 TABLET (60 TABLET) in 1 BOTTLE, PLASTIC None
3 NDC:53489-503-01 100 TABLET (100 TABLET) in 1 BOTTLE, PLASTIC None
4 NDC:53489-503-03 250 TABLET (250 TABLET) in 1 BOTTLE, PLASTIC None
5 NDC:53489-503-05 500 TABLET (500 TABLET) in 1 BOTTLE, PLASTIC None
6 NDC:53489-503-10 1000 TABLET (1000 TABLET) in 1 BOTTLE, PLASTIC None
SOTALOL sotalol tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53489-504
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
sotalol (sotalol) sotalol 120 mg
Inactive Ingredients
Ingredient Name Strength
Anhydrous lactose
colloidal silicon dioxide
corn starch
magnesium stearate
microcrystalline cellulose
pregelatinized starch
sodium starch glycolate
stearic acid
Product Characteristics
Color WHITE Score 2 pieces
Shape OVAL Size 12mm
Flavor Imprint Code MP;519
Contains
Coating false Symbol false
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53489-504-07 30 TABLET (30 TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:53489-504-06 60 TABLET (60 TABLET) in 1 BOTTLE, PLASTIC None
3 NDC:53489-504-01 100 TABLET (100 TABLET) in 1 BOTTLE, PLASTIC None
4 NDC:53489-504-03 250 TABLET (250 TABLET) in 1 BOTTLE, PLASTIC None
5 NDC:53489-504-05 500 TABLET (500 TABLET) in 1 BOTTLE, PLASTIC None
6 NDC:53489-504-10 1000 TABLET (1000 TABLET) in 1 BOTTLE, PLASTIC None
SOTALOL sotalol tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53489-505
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
sotalol (sotalol) sotalol 160 mg
Inactive Ingredients
Ingredient Name Strength
Anhydrous lactose
colloidal silicon dioxide
corn starch
magnesium stearate
microcrystalline cellulose
pregelatinized starch
sodium starch glycolate
stearic acid
Product Characteristics
Color WHITE Score 2 pieces
Shape OVAL Size 14mm
Flavor Imprint Code MP;520
Contains
Coating false Symbol false
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53489-505-07 30 TABLET (30 TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:53489-505-06 60 TABLET (60 TABLET) in 1 BOTTLE, PLASTIC None
3 NDC:53489-505-01 100 TABLET (100 TABLET) in 1 BOTTLE, PLASTIC None
4 NDC:53489-505-03 250 TABLET (250 TABLET) in 1 BOTTLE, PLASTIC None
5 NDC:53489-505-05 500 TABLET (500 TABLET) in 1 BOTTLE, PLASTIC None
6 NDC:53489-505-10 1000 TABLET (1000 TABLET) in 1 BOTTLE, PLASTIC None
Labeler — MUTUAL PHARMACEUTICAL

Revised: 01/2007 MUTUAL PHARMACEUTICAL

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