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NDC 65162-0767-50 Warfarin Sodium 6 mg/1 Details
Warfarin Sodium 6 mg/1
Warfarin Sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. 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: 65162-0767-50Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Warfarin
Product Information
| NDC | 65162-0767 |
|---|---|
| Product ID | 65162-767_3370ee38-9ec0-4b6e-a6db-07d22efb0f81 |
| Associated GPIs | 83200030200317 |
| GCN Sequence Number | 030475 |
| GCN Sequence Number Description | warfarin sodium TABLET 6 MG ORAL |
| HIC3 | M9L |
| HIC3 Description | ANTICOAGULANTS,COUMARIN TYPE |
| GCN | 25798 |
| HICL Sequence Number | 002812 |
| HICL Sequence Number Description | WARFARIN SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | Warfarin Sodium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Warfarin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 6 |
| Active Ingredient Units | mg/1 |
| Substance Name | WARFARIN SODIUM |
| Labeler Name | Amneal Pharmaceuticals LLC |
| Pharmaceutical Class | Vitamin K Antagonist [EPC], Vitamin K Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA202202 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 65162-0767-50 (65162076750)
| NDC Package Code | 65162-767-50 |
|---|---|
| Billing NDC | 65162076750 |
| Package | 500 TABLET in 1 BOTTLE (65162-767-50) |
| Marketing Start Date | 2010-08-16 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |