Product NDC: | 0268-1518 |
Proprietary Name: | AMARANTHUS TUBERCULATUS POLLEN |
Non Proprietary Name: | Water Hemp |
Active Ingredient(s): | .05 g/mL & nbsp; Water Hemp |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0268-1518 |
Labeler Name: | ALK-Abello, Inc. |
Product Type: | NON-STANDARDIZED ALLERGENIC |
FDA Application Number: | BLA103753 |
Marketing Category: | BLA |
Start Marketing Date: | 19650101 |
Package NDC: | 0268-1518-50 |
Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (0268-1518-50) |
NDC Code | 0268-1518-50 |
Proprietary Name | AMARANTHUS TUBERCULATUS POLLEN |
Package Description | 50 mL in 1 VIAL, MULTI-DOSE (0268-1518-50) |
Product NDC | 0268-1518 |
Product Type Name | NON-STANDARDIZED ALLERGENIC |
Non Proprietary Name | Water Hemp |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 19650101 |
Marketing Category Name | BLA |
Labeler Name | ALK-Abello, Inc. |
Substance Name | AMARANTHUS TUBERCULATUS POLLEN |
Strength Number | .05 |
Strength Unit | g/mL |
Pharmaceutical Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |