Product NDC: | 0268-0826 |
Proprietary Name: | ASPERGILLUS FUMIGATUS |
Non Proprietary Name: | ASPERGILLUS FUMIGATUS |
Active Ingredient(s): | 10000 [PNU]/mL & nbsp; ASPERGILLUS FUMIGATUS |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0268-0826 |
Labeler Name: | ALK-Abello, Inc. |
Product Type: | NON-STANDARDIZED ALLERGENIC |
FDA Application Number: | BLA103753 |
Marketing Category: | BLA |
Start Marketing Date: | 19650101 |
Package NDC: | 0268-0826-50 |
Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (0268-0826-50) |
NDC Code | 0268-0826-50 |
Proprietary Name | ASPERGILLUS FUMIGATUS |
Package Description | 50 mL in 1 VIAL, MULTI-DOSE (0268-0826-50) |
Product NDC | 0268-0826 |
Product Type Name | NON-STANDARDIZED ALLERGENIC |
Non Proprietary Name | ASPERGILLUS FUMIGATUS |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 19650101 |
Marketing Category Name | BLA |
Labeler Name | ALK-Abello, Inc. |
Substance Name | ASPERGILLUS FUMIGATUS |
Strength Number | 10000 |
Strength Unit | [PNU]/mL |
Pharmaceutical Classes | Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient] |