NDC 0268-0839
BOTRYTIS CINEREA
Botrytis Cinerea
BOTRYTIS CINEREA is a Subcutaneous Injection, Solution in the Non-standardized Allergenic category. It is labeled and distributed by Alk-abello, Inc.. The primary component is Botrytis Cinerea.
Product ID | 0268-0839_152accc2-8563-4b11-9c7c-f61b002b30f8 |
NDC | 0268-0839 |
Product Type | Non-standardized Allergenic |
Proprietary Name | BOTRYTIS CINEREA |
Generic Name | Botrytis Cinerea |
Dosage Form | Injection, Solution |
Route of Administration | SUBCUTANEOUS |
Marketing Start Date | 1965-01-01 |
Marketing End Date | 2021-11-30 |
Marketing Category | BLA / BLA |
Application Number | BLA103753 |
Labeler Name | ALK-Abello, Inc. |
Substance Name | BOTRYTIS CINEREA |
Active Ingredient Strength | 10000 [PNU]/mL |
Pharm Classes | Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS] |
NDC Exclude Flag | N |