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NDC 71335-1059-02 Warfarin Sodium 7.5 mg/1 Details

Warfarin Sodium 7.5 mg/1

Warfarin Sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is WARFARIN SODIUM.

MedlinePlus Drug Summary

Warfarin is used to prevent blood clots from forming or growing larger in your blood and blood vessels. It is prescribed for people with certain types of irregular heartbeat, people with prosthetic (replacement or mechanical) heart valves, and people who have suffered a heart attack. Warfarin is also used to treat or prevent venous thrombosis (swelling and blood clot in a vein) and pulmonary embolism (a blood clot in the lung). Warfarin is in a class of medications called anticoagulants ('blood thinners'). It works by decreasing the clotting ability of the blood.

Related Packages: 71335-1059-02
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Warfarin

Product Information

NDC	71335-1059
Product ID	71335-1059_2634a3b7-1a57-4f6e-93fa-78e513d0b9b7
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Warfarin Sodium
Proprietary Name Suffix	n/a
Non-Proprietary Name	Warfarin Sodium
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	7.5
Active Ingredient Units	mg/1
Substance Name	WARFARIN SODIUM
Labeler Name	Bryant Ranch Prepack
Pharmaceutical Class	Vitamin K Antagonist [EPC], Vitamin K Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA040616
Listing Certified Through	2024-12-31

Package

NDC 71335-1059-02 (71335105902)

Pricing Information	N/A
NDC Package Code	71335-1059-2
Billing NDC	71335105902
Package	90 TABLET in 1 BOTTLE (71335-1059-2)
Marketing Start Date	2022-02-09
NDC Exclude Flag	N