Orris Root is a Intradermal; Percutaneous; Subcutaneous Solution in the Non-standardized Allergenic category. It is labeled and distributed by Greer Laboratories, Inc.. The primary component is Iris X Germanica Nothovar. Florentina Root.
Product ID | 22840-5515_7a027fdf-a68d-9cbf-e053-2a91aa0ac4d6 |
NDC | 22840-5515 |
Product Type | Non-standardized Allergenic |
Proprietary Name | Orris Root |
Generic Name | Iris Germanica |
Dosage Form | Solution |
Route of Administration | INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS |
Marketing Start Date | 1981-09-15 |
Marketing Category | BLA / BLA |
Application Number | BLA101833 |
Labeler Name | Greer Laboratories, Inc. |
Substance Name | IRIS X GERMANICA NOTHOVAR. FLORENTINA ROOT |
Active Ingredient Strength | 0 g/mL |
Pharm Classes | Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Plant Proteins [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 1981-09-15 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA101833 |
Product Type | NON-STANDARDIZED ALLERGENIC |
Marketing Start Date | 1981-09-15 |
Marketing Category | BLA |
Application Number | BLA101833 |
Product Type | NON-STANDARDIZED ALLERGENIC |
Marketing Start Date | 1981-09-15 |
Ingredient | Strength |
---|---|
IRIS X GERMANICA NOTHOVAR. FLORENTINA ROOT | .025 g/mL |
NDC | Brand Name | Generic Name |
---|---|---|
22840-1530 | Orris Root | Iris germanica |
22840-1531 | Orris Root | Iris germanica |
22840-5515 | Orris Root | Iris germanica |
36987-2234 | Orris Root | Orris Root |
36987-2235 | Orris Root | Orris Root |
36987-2236 | Orris Root | Orris Root |
36987-2237 | Orris Root | Orris Root |
49288-0343 | Orris Root | Orris Root |
49288-0344 | Orris Root | Orris Root |
49643-020 | Orris Root | Orris Root |
54575-272 | ORRIS ROOT | iris germanica var. florentina root |