Warfarin Sodium (Page 9 of 9)

Label Image for 1mg

Label Image for 1mg
(click image for full-size original)

Label Image for 2mg

Label Image for 2mg
(click image for full-size original)

Label Image for 2.5mg

Label Image for 2.5mg
(click image for full-size original)

Label Image for 3mg

Label Image for 3mg
(click image for full-size original)

Label Image for 5mg

Label Image for 5mg
(click image for full-size original)

Label Image for 7.5mg

Label Image for 7.5mg
(click image for full-size original)

Label Image for 10mg

Label Image for 10mg
(click image for full-size original)
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53808-0985(NDC:51672-4027)
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
ANHYDROUS LACTOSE
STARCH, CORN
MAGNESIUM STEARATE
D&C RED NO. 6
Product Characteristics
Color pink Score 2 pieces
Shape OVAL Size 11mm
Flavor Imprint Code 1;WARFARIN;TARO
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53808-0985-1 30 TABLET (TABLET) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040301 07/01/2009
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53808-0335(NDC:51672-4028)
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
ANHYDROUS LACTOSE
STARCH, CORN
MAGNESIUM STEARATE
FD&C BLUE NO. 2
FD&C RED NO. 40
Product Characteristics
Color purple (Lavendar) Score 2 pieces
Shape OVAL Size 11mm
Flavor Imprint Code 2;WARFARIN;TARO
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53808-0335-1 30 TABLET (TABLET) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040301 07/01/2009
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53808-0994(NDC:51672-4029)
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
ANHYDROUS LACTOSE
STARCH, CORN
MAGNESIUM STEARATE
FD&C BLUE NO. 2
D&C YELLOW NO. 10
Product Characteristics
Color green Score 2 pieces
Shape OVAL Size 11mm
Flavor Imprint Code 2;12;WARFARIN;TARO
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53808-0994-1 30 TABLET (TABLET) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040301 07/01/2009
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53808-0334(NDC:51672-4030)
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
ANHYDROUS LACTOSE
STARCH, CORN
MAGNESIUM STEARATE
FD&C BLUE NO. 2
FD&C RED NO. 40
D&C YELLOW NO. 10
Product Characteristics
Color brown (tan) Score 2 pieces
Shape OVAL Size 11mm
Flavor Imprint Code 3;WARFARIN;TARO
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53808-0334-1 30 TABLET (TABLET) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040301 07/01/2009
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53808-0970(NDC:51672-4032)
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
ANHYDROUS LACTOSE
STARCH, CORN
MAGNESIUM STEARATE
D&C YELLOW NO. 10
D&C RED NO. 6
Product Characteristics
Color orange (peach) Score 2 pieces
Shape OVAL Size 11mm
Flavor Imprint Code 5;WARFARIN;TARO
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53808-0970-1 30 TABLET (TABLET) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040301 07/01/2009
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53808-0997(NDC:51672-4034)
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
ANHYDROUS LACTOSE
STARCH, CORN
MAGNESIUM STEARATE
D&C YELLOW NO. 10
Product Characteristics
Color yellow Score 2 pieces
Shape OVAL Size 11mm
Flavor Imprint Code 7;12;WARFARIN;TARO
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53808-0997-1 30 TABLET (TABLET) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040301 07/01/2009
WARFARIN SODIUM warfarin sodium tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53808-0989(NDC:51672-4035)
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
ANHYDROUS LACTOSE
STARCH, CORN
MAGNESIUM STEARATE
Product Characteristics
Color white Score 2 pieces
Shape OVAL Size 11mm
Flavor Imprint Code 10;WARFARIN;TARO
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53808-0989-1 30 TABLET (TABLET) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040301 07/01/2009
Labeler — State of Florida DOH Central Pharmacy (829348114)
Establishment
Name Address ID/FEI Operations
State of Florida DOH Central Pharmacy 829348114 repack

Revised: 06/2010 State of Florida DOH Central Pharmacy

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2020. All Rights Reserved.