Sunflower Pollen is a Cutaneous; Intradermal; Subcutaneous Injection in the Non-standardized Allergenic category. It is labeled and distributed by Allermed Laboratories, Inc.. The primary component is Helianthus Annuus Pollen.
| Product ID | 49643-360_4f1be4f6-9f9e-5c19-e054-00144ff8d46c |
| NDC | 49643-360 |
| Product Type | Non-standardized Allergenic |
| Proprietary Name | Sunflower Pollen |
| Generic Name | Helianthus Annua |
| Dosage Form | Injection |
| Route of Administration | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1974-03-12 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102211 |
| Labeler Name | Allermed Laboratories, Inc. |
| Substance Name | HELIANTHUS ANNUUS POLLEN |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 1974-03-12 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | BLA |
| Application Number | BLA102211 |
| Product Type | NON-STANDARDIZED ALLERGENIC |
| Marketing Start Date | 1974-03-12 |
| Marketing Category | BLA |
| Application Number | BLA102211 |
| Product Type | NON-STANDARDIZED ALLERGENIC |
| Marketing Start Date | 1974-03-12 |
| Marketing Category | BLA |
| Application Number | BLA102211 |
| Product Type | NON-STANDARDIZED ALLERGENIC |
| Marketing Start Date | 1974-03-12 |
| Marketing Category | BLA |
| Application Number | BLA102211 |
| Product Type | NON-STANDARDIZED ALLERGENIC |
| Marketing Start Date | 1974-03-12 |
| Ingredient | Strength |
|---|---|
| HELIANTHUS ANNUUS POLLEN | .05 g/mL |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 49288-0490 | Sunflower Pollen | Sunflower Pollen |
| 49643-360 | Sunflower Pollen | Helianthus annua |
| 54575-179 | SUNFLOWER POLLEN | helianthus annuus pollen |