NDC 22840-2662
Botrytis cinerea
Botrytis Cinerea
Botrytis cinerea 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 Botrytis Cinerea.
Product ID | 22840-2662_77436178-2957-6a77-e053-2a91aa0a873e |
NDC | 22840-2662 |
Product Type | Non-standardized Allergenic |
Proprietary Name | Botrytis cinerea |
Generic Name | Botrytis Cinerea |
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 | 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 | N |
Listing Certified Through | 2019-12-31 |