NDC 36987-1909
Botrytis cinerea
Botrytis Cinerea
Botrytis cinerea is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Botrytis Cinerea.
Product ID | 36987-1909_9ea18f57-b968-4c63-84f4-9e6ae475d10f |
NDC | 36987-1909 |
Product Type | Human Prescription Drug |
Proprietary Name | Botrytis cinerea |
Generic Name | Botrytis Cinerea |
Dosage Form | Injection, Solution |
Route of Administration | INTRADERMAL; SUBCUTANEOUS |
Marketing Start Date | 1972-08-29 |
Marketing Category | BLA / BLA |
Application Number | BLA102192 |
Labeler Name | Nelco Laboratories, Inc. |
Substance Name | BOTRYTIS CINEREA |
Active Ingredient Strength | 0 g/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 | E |
Listing Certified Through | 2017-12-31 |