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Warfarin Sodium 6 MG Oral Tablet

1 INDICATIONS AND USAGE Warfarin sodium tablets are indicated for: Prophylaxis and treatment of venous thrombosis and its extension, pulmonary embolism (PE). Prophylaxis and treatment of thromboembolic complications associated with atrial fibrillation (AF) and/or cardiac valve replacement. Reduction in the risk of death, recurrent myocardial infarction (MI), and thromboembolic events such as stroke or systemic embolization after myocardial infarction. Limitations of Use Warfarin sodium tablets have no direct effect on an established thrombus, nor does it reverse ischemic tissue damage. Once a thrombus has occurred, however, the goals of anticoagulant treatment are to prevent further extension of the formed clot and to prevent secondary thromboembolic complications that may result in serious and possibly fatal sequelae. Warfarin sodium tablets are a vitamin K antagonist indicated for: Prophylaxis and treatment of venous thrombosis and its extension, pulmonary embolism ( 1 ) Prophylaxis and treatment of thromboembolic complications associated with atrial fibrillation and/or cardiac valve replacement ( 1 ) Reduction in the risk of death, recurrent myocardial infarction, and thromboembolic events such as stroke or systemic embolization after myocardial infarction ( 1 ) Limitations of Use Warfarin sodium tablets have no direct effect on an established thrombus, nor does it reverse ischemic tissue damage. ( 1 )

Teva Pharmaceuticals USA, Inc.


3 years ago OVAL TURQUOISE TV 6 1718 Warfarin Sodium 6 MG Oral Tablet

OVAL TURQUOISE TV 6 1718

3 years ago OVAL TURQUOISE TV 6 1718 Warfarin Sodium 6 MG Oral Tablet

TV 6 1718 OVAL TURQUOISE

16 HOW SUPPLIED/STORAGE AND HANDLING

WARFARIN SODIUM tablets USP, 1 mg are available as pink, capsule-shaped, biconvex scored tablets, debossed with TV/1 on the scored side and 1712 on the other side containing 1 mg

WARFARIN SODIUM, USP, packaged in bottles of 100 (NDC 0093-1712-01) and 1000 (NDC 0093-1712-10) tablets.

WARFARIN SODIUM tablets USP, 2 mg are available as Lavender, capsule-shaped, biconvex scored tablets, debossed with TV/2 on the scored side and 1713 on the other side containing 2 mg

WARFARIN SODIUM, USP, packaged in bottles of 100 (NDC 0093-1713-01) and 1000 (NDC 0093-1713-10) tablets.

WARFARIN SODIUM tablets USP, 2.5 mg are available as green, capsule-shaped, biconvex scored tablets, debossed with TV/2 1 / 2 on the scored side and 1714 on the other side containing 2.5 mg

WARFARIN SODIUM, USP, packaged in bottles of 100 (NDC 0093-1714-01) and 1000 (NDC 0093-1714-10) tablets.

WARFARIN SODIUM tablets USP, 3 mg are available as tan, capsule-shaped, biconvex scored tablets, debossed with TV/3 on the scored side and 1715 on the other side containing 3 mg

WARFARIN SODIUM, USP, packaged in bottles of 100 (NDC 0093-1715-01) tablets.

WARFARIN SODIUM tablets USP, 4 mg are available as blue, capsule-shaped, biconvex scored tablets, debossed with TV/4 on the scored side and 1716 on the other side containing 4 mg

WARFARIN SODIUM, USP, packaged in bottles of 100 (NDC 0093-1716-01) and 1000 (NDC 0093-1716-10) tablets.

WARFARIN SODIUM tablets USP, 5 mg are available as peach, capsule-shaped, biconvex scored tablets, debossed with TV/5 on the scored side and 1721 on the other side containing 5 mg

WARFARIN SODIUM, USP, packaged in bottles of 100 (NDC 0093-1721-01) and 1000 (NDC 0093-1721-10) tablets.

WARFARIN SODIUM tablets USP, 6 mg are available as teal, capsule-shaped, biconvex scored tablets, debossed with TV/6 on the scored side and 1718 on the other side containing 6 mg

WARFARIN SODIUM, USP, packaged in bottles of 100 (NDC 0093-1718-01) tablets.

WARFARIN SODIUM tablets USP, 7.5 mg are available as yellow, capsule-shaped, biconvex scored tablets, debossed with TV/7 1 / 2 on the scored side and 1719 on the other side containing 7.5 mg

WARFARIN SODIUM, USP, packaged in bottles of 100 (NDC 0093-1723-01) tablets.

WARFARIN SODIUM tablets USP, 10 mg are available as white, capsule-shaped, biconvex scored tablets, debossed with TV/10 on the scored side and 1720 on the other side containing 10 mg

WARFARIN SODIUM, USP, packaged in bottles of 100 (NDC 0093-1720-01) tablets. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required). Protect from light. Keep tightly closed. Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Special Handling Procedures for proper handling and disposal of potentially hazardous drugs should be considered. Guidelines on this subject have been published [see References ( 15 )] . Pharmacy and clinical personnel who are pregnant should avoid exposure to crushed or broken tablets [see Use in Specific Populations ( 8.1 )] . KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

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