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 |