Viekira XR is a Kit in the Human Prescription Drug category. It is labeled and distributed by Abbvie Inc.. The primary component is .
Product ID | 0074-0063_281213a0-74d6-b252-2ed8-459ee77152e7 |
NDC | 0074-0063 |
Product Type | Human Prescription Drug |
Proprietary Name | Viekira XR |
Generic Name | Dasabuvir And Ombitasvir And Paritaprevir And Ritonavir |
Dosage Form | Kit |
Marketing Start Date | 2016-07-22 |
Marketing Category | NDA / NDA |
Application Number | NDA208624 |
Labeler Name | AbbVie Inc. |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2016-07-22 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA208624 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-07-22 |
Marketing End Date | 2019-01-17 |
Marketing Category | NDA |
Application Number | NDA208624 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-07-22 |
Marketing End Date | 2019-01-17 |
SPL SET ID: | 2e9dc175-80cb-b598-d035-4c3d5134c096 |
Manufacturer | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0074-0063 | Viekira | Dasabuvir and Ombitasvir and Paritaprevir and Ritonavir |
0074-3093 | Viekira Pak | Dasabuvir and Ombitasvir and Paritaprevir and Ritonavir |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VIEKIRA 86039507 not registered Dead/Abandoned |
AbbVie Inc. 2013-08-15 |