NDC 36987-1870
Aspergillus flavus
Aspergillus Flavus
Aspergillus flavus 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 Aspergillus Flavus.
Product ID | 36987-1870_9010bf62-c443-49a9-b8f8-fa8dd9223885 |
NDC | 36987-1870 |
Product Type | Human Prescription Drug |
Proprietary Name | Aspergillus flavus |
Generic Name | Aspergillus Flavus |
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 | ASPERGILLUS FLAVUS |
Active Ingredient Strength | 40000 [PNU]/mL |
Pharm Classes | Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Fungal Proteins [CS],Allergens [CS] |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |