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NDC 65597-0202-07 SAVAYSA 30 mg/1 Details
SAVAYSA 30 mg/1
SAVAYSA is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Daiichi Sankyo. The primary component is EDOXABAN TOSYLATE.
MedlinePlus Drug Summary
Edoxaban is used help prevent strokes or blood clots in people who have atrial fibrillation (a condition in which the heart beats irregularly, increasing the chance of clots forming in the body and possibly causing strokes) that is not caused by heart valve disease. Edoxaban is also used to prevent deep vein thrombosis (DVT; a blood clot, usually in the leg) and pulmonary embolism (PE; a blood clot in the lung) in people who have been treated with an injectable blood thinner medicine for 5 to 10 days. Edoxaban is in a class of medications called factor Xa inhibitors. It works by blocking the action of a certain natural substance that helps blood clots to form.
Related Packages: 65597-0202-07Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Edoxaban
Product Information
| NDC | 65597-0202 |
|---|---|
| Product ID | 65597-202_ecdf9b93-99ef-4356-a6cc-15d04a4b28c4 |
| Associated GPIs | 83370030200330 |
| GCN Sequence Number | 073294 |
| GCN Sequence Number Description | edoxaban tosylate TABLET 30 MG ORAL |
| HIC3 | M9V |
| HIC3 Description | DIRECT FACTOR XA INHIBITORS |
| GCN | 37676 |
| HICL Sequence Number | 041672 |
| HICL Sequence Number Description | EDOXABAN TOSYLATE |
| Brand/Generic | Brand |
| Proprietary Name | SAVAYSA |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | EDOXABAN TOSYLATE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 30 |
| Active Ingredient Units | mg/1 |
| Substance Name | EDOXABAN TOSYLATE |
| Labeler Name | Daiichi Sankyo |
| Pharmaceutical Class | Factor Xa Inhibitor [EPC], Factor Xa Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA206316 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 65597-0202-07 (65597020207)
| NDC Package Code | 65597-202-07 |
|---|---|
| Billing NDC | 65597020207 |
| Package | 7 TABLET, FILM COATED in 1 BOTTLE (65597-202-07) |
| Marketing Start Date | 2015-01-31 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |