NDC 54575-463
SUNFLOWER SEED
Sunflower Seed
SUNFLOWER SEED 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 Sunflower Seed.
Product ID | 54575-463_dbe7bebd-e445-4e59-8302-e706b795fbde |
NDC | 54575-463 |
Product Type | Human Prescription Drug |
Proprietary Name | SUNFLOWER SEED |
Generic Name | Sunflower Seed |
Dosage Form | Injection, Solution |
Route of Administration | PERCUTANEOUS; SUBCUTANEOUS |
Marketing Start Date | 1972-08-29 |
Marketing Category | BLA / BLA |
Application Number | BLA102192 |
Labeler Name | Allergy Laboratories, Inc. |
Substance Name | SUNFLOWER SEED |
Active Ingredient Strength | 1 g/20mL |
Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Seed Storage Proteins [CS],Plant Proteins [CS] |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |