UBRELVY is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Allergan, Inc.. The primary component is Ubrogepant.
Product ID | 0023-6498_179b083b-faaf-4092-9f87-005dab651067 |
NDC | 0023-6498 |
Product Type | Human Prescription Drug |
Proprietary Name | UBRELVY |
Generic Name | Ubrogepant |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2019-12-23 |
Marketing Category | NDA / NDA |
Application Number | NDA211765 |
Labeler Name | Allergan, Inc. |
Substance Name | UBROGEPANT |
Active Ingredient Strength | 50 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2019-12-23 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA211765 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-12-23 |
Marketing Category | NDA |
Application Number | NDA211765 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-12-23 |
Marketing Category | NDA |
Application Number | NDA211765 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-12-23 |
Marketing Category | NDA |
Application Number | NDA211765 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2019-12-23 |
Marketing Category | NDA |
Application Number | NDA211765 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-12-23 |
Marketing Category | NDA |
Application Number | NDA211765 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2019-12-23 |
Ingredient | Strength |
---|---|
UBROGEPANT | 50 mg/1 |
NDC | Brand Name | Generic Name |
---|---|---|
0023-6498 | UBRELVY | ubrogepant |
0023-6501 | UBRELVY | ubrogepant |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
UBRELVY 88185227 not registered Live/Pending |
Allergan Pharmaceuticals International Limited 2018-11-07 |
UBRELVY 88155130 not registered Live/Pending |
ALLERGAN PHARMACEUTICALS INTERNATIONAL LIMITED 2018-10-15 |