NDC 22840-5410
American Beech Pollen
Fagus Grandifolia
American Beech Pollen 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 Fagus Grandifolia Pollen.
Product ID | 22840-5410_83d281e9-375b-7e6c-e053-2991aa0a6f0e |
NDC | 22840-5410 |
Product Type | Non-standardized Allergenic |
Proprietary Name | American Beech Pollen |
Generic Name | Fagus Grandifolia |
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 | FAGUS GRANDIFOLIA POLLEN |
Active Ingredient Strength | 0 g/mL |
Pharm Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |