Warfarin Sodium (Page 9 of 9)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rising NDC 57237-119-01

Warfarin Sodium

Tablets, USP

Crystalline* 1 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

100 Tablets Rx only

1 MG-100 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-119-99

Warfarin Sodium

Tablets, USP

Crystalline* 1 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

1000 Tablets Rx only

1 MG-1000 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-120-01

Warfarin Sodium

Tablets, USP

Crystalline* 2 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

100 Tablets Rx only

2 MG-100 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-120-99

Warfarin Sodium

Tablets, USP

Crystalline* 2 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

1000 Tablets Rx only

2 MG-1000 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-121-01

Warfarin Sodium

Tablets, USP

Crystalline* 2.5 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

100 Tablets Rx only

2.5 MG-100 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-121-99

Warfarin Sodium

Tablets, USP

Crystalline* 2.5 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

1000 Tablets Rx only

2.5 MG-1000 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-122-01

Warfarin Sodium

Tablets, USP

Crystalline* 3 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

100 Tablets Rx only

3 MG-100 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-122-99

Warfarin Sodium

Tablets, USP

Crystalline* 3 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

1000 Tablets Rx only

3 MG-1000 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-123-01

Warfarin Sodium

Tablets, USP

Crystalline* 4 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

100 Tablets Rx only

4 MG-100 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-123-99

Warfarin Sodium

Tablets, USP

Crystalline* 4 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

1000 Tablets Rx only

4 MG-1000 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-124-01

Warfarin Sodium

Tablets, USP

Crystalline* 5 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

100 Tablets Rx only

5 MG-100 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-124-99

Warfarin Sodium

Tablets, USP

Crystalline* 5 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

1000 Tablets Rx only

5 MG-1000 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-125-01

Warfarin Sodium

Tablets, USP

Crystalline* 6 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

100 Tablets Rx only

6 MG-100 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-126-01

Warfarin Sodium

Tablets, USP

Crystalline* 7.5 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

100 Tablets Rx only

7.5 MG-100 COUNT LABEL
(click image for full-size original)

Rising NDC 57237-127-01

Warfarin Sodium

Tablets, USP

Crystalline* 10 mg

PHARMACIST: Dispense the Medication Guide provided separately to each patient.

HIGHLY POTENT ANTI COAGULANT

WARNING: Serious bleeding results from overdosage. Do not use or dispense before reading directions and warnings in accompanying product information.

100 Tablets Rx only

10 MG-100 COUNT LABEL
(click image for full-size original)
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57237-119
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WARFARIN SODIUM (WARFARIN) WARFARIN SODIUM 1 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
HYDROXYPROPYL CELLULOSE
D&C RED NO. 30
Product Characteristics
Color PINK (Light Pink) Score 2 pieces
Shape ROUND (Flat Beveled Edge) Size 8mm
Flavor Imprint Code I;G;W;1
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57237-119-01 100 TABLET in 1 BOTTLE None
2 NDC:57237-119-99 1000 TABLET in 1 BOTTLE None
3 NDC:57237-119-90 90 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090935 11/11/2011
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57237-120
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WARFARIN SODIUM (WARFARIN) WARFARIN SODIUM 2 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
HYDROXYPROPYL CELLULOSE
FD&C BLUE NO. 2
FD&C RED NO. 40
Product Characteristics
Color PURPLE (Lavender) Score 2 pieces
Shape ROUND (Flat Beveled Edge) Size 8mm
Flavor Imprint Code I;G;W;2
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57237-120-99 1000 TABLET in 1 BOTTLE None
2 NDC:57237-120-90 90 TABLET in 1 BOTTLE None
3 NDC:57237-120-01 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090935 11/11/2011
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57237-121
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WARFARIN SODIUM (WARFARIN) WARFARIN SODIUM 2.5 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
HYDROXYPROPYL CELLULOSE
FD&C BLUE NO. 2
D&C YELLOW NO. 10
Product Characteristics
Color GREEN (Green) Score 2 pieces
Shape ROUND (Flat Beveled Edge) Size 8mm
Flavor Imprint Code I;G;W;2;1;2
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57237-121-99 1000 TABLET in 1 BOTTLE None
2 NDC:57237-121-90 90 TABLET in 1 BOTTLE None
3 NDC:57237-121-01 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090935 11/11/2011
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57237-122
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WARFARIN SODIUM (WARFARIN) WARFARIN SODIUM 3 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
HYDROXYPROPYL CELLULOSE
FD&C RED NO. 40
FD&C YELLOW NO. 6
FD&C BLUE NO. 2
Product Characteristics
Color BROWN (Tan) Score 2 pieces
Shape ROUND (Flat Beveled Edge) Size 8mm
Flavor Imprint Code I;G;W;3
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57237-122-99 1000 TABLET in 1 BOTTLE None
2 NDC:57237-122-90 90 TABLET in 1 BOTTLE None
3 NDC:57237-122-01 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090935 11/11/2011
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57237-123
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WARFARIN SODIUM (WARFARIN) WARFARIN SODIUM 4 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
HYDROXYPROPYL CELLULOSE
FD&C BLUE NO. 2
Product Characteristics
Color BLUE (Blue) Score 2 pieces
Shape ROUND (Flat Beveled Edge) Size 8mm
Flavor Imprint Code I;G;W;4
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57237-123-99 1000 TABLET in 1 BOTTLE None
2 NDC:57237-123-90 90 TABLET in 1 BOTTLE None
3 NDC:57237-123-01 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090935 11/11/2011
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57237-124
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WARFARIN SODIUM (WARFARIN) WARFARIN SODIUM 5 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
HYDROXYPROPYL CELLULOSE
FD&C YELLOW NO. 6
Product Characteristics
Color PINK (Peach) Score 2 pieces
Shape ROUND (Flat Beveled Edge) Size 8mm
Flavor Imprint Code I;G;W;5
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57237-124-99 1000 TABLET in 1 BOTTLE None
2 NDC:57237-124-90 90 TABLET in 1 BOTTLE None
3 NDC:57237-124-01 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090935 11/11/2011
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57237-125
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WARFARIN SODIUM (WARFARIN) WARFARIN SODIUM 6 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
HYDROXYPROPYL CELLULOSE
FD&C YELLOW NO. 6
FD&C BLUE NO. 2
Product Characteristics
Color TURQUOISE (Teal) Score 2 pieces
Shape ROUND (Flat Beveled Edge) Size 8mm
Flavor Imprint Code I;G;W;6
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57237-125-99 1000 TABLET in 1 BOTTLE None
2 NDC:57237-125-90 90 TABLET in 1 BOTTLE None
3 NDC:57237-125-01 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090935 11/11/2011
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57237-126
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WARFARIN SODIUM (WARFARIN) WARFARIN SODIUM 7.5 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
HYDROXYPROPYL CELLULOSE
FD&C YELLOW NO. 6
D&C YELLOW NO. 10
Product Characteristics
Color YELLOW (Yellow) Score 2 pieces
Shape ROUND (Flat Beveled Edge) Size 8mm
Flavor Imprint Code I;G;W;7;1;2
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57237-126-99 1000 TABLET in 1 BOTTLE None
2 NDC:57237-126-90 90 TABLET in 1 BOTTLE None
3 NDC:57237-126-01 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090935 11/11/2011
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:57237-127
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WARFARIN SODIUM (WARFARIN) WARFARIN SODIUM 10 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
HYDROXYPROPYL CELLULOSE
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND (Flat Beveled Edge) Size 8mm
Flavor Imprint Code I;G;W;10
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:57237-127-99 1000 TABLET in 1 BOTTLE None
2 NDC:57237-127-90 90 TABLET in 1 BOTTLE None
3 NDC:57237-127-01 100 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090935 11/11/2011
Labeler — Rising Health, LLC (080500961)
Establishment
Name Address ID/FEI Operations
InvaGen Pharmaceuticals, Inc 165104469 ANALYSIS (57237-120), ANALYSIS (57237-121), ANALYSIS (57237-122), ANALYSIS (57237-123), ANALYSIS (57237-124), ANALYSIS (57237-125), ANALYSIS (57237-126), ANALYSIS (57237-127), MANUFACTURE (57237-119), MANUFACTURE (57237-120), MANUFACTURE (57237-121), MANUFACTURE (57237-122), MANUFACTURE (57237-123), MANUFACTURE (57237-124), MANUFACTURE (57237-125), MANUFACTURE (57237-126), MANUFACTURE (57237-127)

Revised: 07/2018 Rising Health, LLC

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