NDC 54575-179
SUNFLOWER POLLEN
Helianthus Annuus Pollen
SUNFLOWER POLLEN is a Percutaneous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Allergy Laboratories, Inc.. The primary component is Helianthus Annuus Pollen.
Product ID | 54575-179_dbe7bebd-e445-4e59-8302-e706b795fbde |
NDC | 54575-179 |
Product Type | Human Prescription Drug |
Proprietary Name | SUNFLOWER POLLEN |
Generic Name | Helianthus Annuus Pollen |
Dosage Form | Injection, Solution |
Route of Administration | PERCUTANEOUS; SUBCUTANEOUS |
Marketing Start Date | 1967-12-07 |
Marketing Category | BLA / BLA |
Application Number | BLA101376 |
Labeler Name | Allergy Laboratories, Inc. |
Substance Name | HELIANTHUS ANNUUS POLLEN |
Active Ingredient Strength | 1 g/20mL |
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 | E |
Listing Certified Through | 2018-12-31 |