dule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Warfarin Sodium(Warfarin) Warfarin Sodium 3mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STEARIC ACID
FD&C YELLOW NO. 6
FD&C BLUE NO. 2
FD&C RED NO. 40
Product Characteristics
Color WHITE (beige) Score 2pieces
Shape ROUND Size 9mm
Flavor Imprint Code WF;3;G
Contains
Packaging
# NDC Package Description Multilevel Packaging
1 51138-198-30 30TABLETIn1BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040415 01/20/2011
WARFARIN SODIUM
warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 51138-199(0378-8804)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Warfarin Sodium(Warfarin) Warfarin Sodium 4mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STEARIC ACID
FD&C BLUE NO. 1
Product Characteristics
Color BLUE Score 2pieces
Shape ROUND Size 9mm
Flavor Imprint Code WF;4;G
Contains
Packaging
# NDC Package Description Multilevel Packaging
1 51138-199-30 30TABLETIn1BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040415 01/20/2011
WARFARIN SODIUM
warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 51138-200(0378-8805)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Warfarin Sodium(Warfarin) Warfarin Sodium 5mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STEARIC ACID
FD&C YELLOW NO. 6
Product Characteristics
Color ORANGE (peach) Score 2pieces
Shape ROUND Size 9mm
Flavor Imprint Code WF;5;G
Contains
Packaging
# NDC Package Description Multilevel Packaging
1 51138-200-30 30TABLETIn1BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040415 01/20/2011
WARFARIN SODIUM
warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 51138-201(0378-8806)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Warfarin Sodium(Warfarin) Warfarin Sodium 6mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
