NDC 65597-202
SAVAYSA
Edoxaban Tosylate
SAVAYSA is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Daiichi Sankyo Inc.. The primary component is Edoxaban Tosylate.
| Product ID | 65597-202_6c185299-f1a9-4224-8e25-d3d04f0fe764 |
| NDC | 65597-202 |
| Product Type | Human Prescription Drug |
| Proprietary Name | SAVAYSA |
| Generic Name | Edoxaban Tosylate |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-01-12 |
| Marketing Category | NDA / NDA |
| Application Number | NDA206316 |
| Labeler Name | Daiichi Sankyo Inc. |
| Substance Name | EDOXABAN TOSYLATE |
| Active Ingredient Strength | 30 mg/1 |
| Pharm Classes | Factor Xa Inhibitor [EPC],Factor Xa Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
Packaging
NDC 65597-202-05
50 BLISTER PACK in 1 CARTON (65597-202-05) > 1 TABLET, FILM COATED in 1 BLISTER PACK
| Marketing Start Date | 2015-01-31 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 65597-202-05 [65597020205]
SAVAYSA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA206316 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-01-31 |
NDC 65597-202-07 [65597020207]
SAVAYSA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA206316 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-01-31 |
NDC 65597-202-50 [65597020250]
SAVAYSA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA206316 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-01-31 |
NDC 65597-202-90 [65597020290]
SAVAYSA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA206316 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-01-31 |
NDC 65597-202-70 [65597020270]
SAVAYSA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA206316 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-01-31 |
NDC 65597-202-10 [65597020210]
SAVAYSA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA206316 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-01-31 |
NDC 65597-202-30 [65597020230]
SAVAYSA TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA206316 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-01-31 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| EDOXABAN TOSYLATE | 30 mg/1 |
OpenFDA Data
| SPL SET ID: | e77d3400-56ad-11e3-949a-0800200c9a66 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
Pharmacological Class
- Factor Xa Inhibitor [EPC]
- Factor Xa Inhibitors [MoA]
Medicade Reported Pricing
65597020290 SAVAYSA 30 MG TABLET
Pricing Unit: EA | Drug Type:
65597020230 SAVAYSA 30 MG TABLET
Pricing Unit: EA | Drug Type:
65597020205 SAVAYSA 30 MG TABLET
Pricing Unit: EA | Drug Type:
NDC Crossover Matching brand name "SAVAYSA" or generic name "Edoxaban Tosylate"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 65597-201 | SAVAYSA | EDOXABAN TOSYLATE |
| 65597-202 | SAVAYSA | EDOXABAN TOSYLATE |
| 65597-203 | SAVAYSA | EDOXABAN TOSYLATE |
Trademark Results [SAVAYSA]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SAVAYSA 85972672 4964909 Live/Registered |
DAIICHI SANKYO COMPANY, LIMITED 2013-06-28 |
 SAVAYSA 85837649 not registered Dead/Abandoned |
DAIICHI SANKYO COMPANY, LIMITED 2013-01-31 |
 SAVAYSA 85627211 4752223 Live/Registered |
DAIICHI SANKYO COMPANY, LIMITED 2012-05-16 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.