Product NDC: | 65044-2315 |
Proprietary Name: | Pollens - Weeds and Garden Plants, Ragweed, Mixed Ambrosia |
Non Proprietary Name: | Ragweed, Mixed Ambrosia |
Active Ingredient(s): | .05; .05 g/mL; g/mL & nbsp; Ragweed, Mixed Ambrosia |
Administration Route(s): | PERCUTANEOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65044-2315 |
Labeler Name: | Jubilant HollisterStier LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103888 |
Marketing Category: | BLA |
Start Marketing Date: | 19410419 |
Package NDC: | 65044-2315-1 |
Package Description: | 5 mL in 1 VIAL (65044-2315-1) |
NDC Code | 65044-2315-1 |
Proprietary Name | Pollens - Weeds and Garden Plants, Ragweed, Mixed Ambrosia |
Package Description | 5 mL in 1 VIAL (65044-2315-1) |
Product NDC | 65044-2315 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ragweed, Mixed Ambrosia |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | PERCUTANEOUS; SUBCUTANEOUS |
Start Marketing Date | 19410419 |
Marketing Category Name | BLA |
Labeler Name | Jubilant HollisterStier LLC |
Substance Name | AMBROSIA ARTEMISIIFOLIA POLLEN; AMBROSIA TRIFIDA POLLEN |
Strength Number | .05; .05 |
Strength Unit | g/mL; g/mL |
Pharmaceutical Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient],Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |