ORRIS is a Percutaneous Injection, Solution in the Non-standardized Allergenic category. It is labeled and distributed by Alk-abello, Inc.. The primary component is Iris X Germanica Root.
Product ID | 0268-6317_06c812ac-2bfd-444c-b2b9-50076167486c |
NDC | 0268-6317 |
Product Type | Non-standardized Allergenic |
Proprietary Name | ORRIS |
Generic Name | Iris X Germanica Root |
Dosage Form | Injection, Solution |
Route of Administration | PERCUTANEOUS |
Marketing Start Date | 1965-01-01 |
Marketing Category | BLA / BLA |
Application Number | BLA103753 |
Labeler Name | ALK-Abello, Inc. |
Substance Name | IRIS X GERMANICA ROOT |
Active Ingredient Strength | 0 g/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 1965-01-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA103753 |
Product Type | NON-STANDARDIZED ALLERGENIC |
Marketing Start Date | 1965-01-01 |
Ingredient | Strength |
---|---|
IRIS X GERMANICA ROOT | .05 g/mL |
NDC | Brand Name | Generic Name |
---|---|---|
0268-0642 | ORRIS | IRIS X GERMANICA ROOT |
0268-6317 | ORRIS | IRIS X GERMANICA ROOT |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ORRIS 97389914 not registered Live/Pending |
Westwood Footwear Corporation 2022-04-29 |