Product NDC: | 65044-1518 |
Proprietary Name: | Pollens - Weeds, Dock/Sorrel Mix |
Non Proprietary Name: | Pollens - Weeds, Dock/Sorrel Mix |
Active Ingredient(s): | 500; 500 [PNU]/mL; [PNU]/mL & nbsp; Pollens - Weeds, Dock/Sorrel Mix |
Administration Route(s): | INTRADERMAL |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65044-1518 |
Labeler Name: | Jubilant HollisterStier LLC |
Product Type: | NON-STANDARDIZED ALLERGENIC |
FDA Application Number: | BLA103888 |
Marketing Category: | BLA |
Start Marketing Date: | 19410419 |
Package NDC: | 65044-1518-5 |
Package Description: | 5 mL in 1 VIAL (65044-1518-5) |
NDC Code | 65044-1518-5 |
Proprietary Name | Pollens - Weeds, Dock/Sorrel Mix |
Package Description | 5 mL in 1 VIAL (65044-1518-5) |
Product NDC | 65044-1518 |
Product Type Name | NON-STANDARDIZED ALLERGENIC |
Non Proprietary Name | Pollens - Weeds, Dock/Sorrel Mix |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRADERMAL |
Start Marketing Date | 19410419 |
Marketing Category Name | BLA |
Labeler Name | Jubilant HollisterStier LLC |
Substance Name | RUMEX ACETOSELLA POLLEN; RUMEX CRISPUS POLLEN |
Strength Number | 500; 500 |
Strength Unit | [PNU]/mL; [PNU]/mL |
Pharmaceutical Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Pollen Allergenic Extract [EPC],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Increased Histamine Release [PE],Allergens [Chemical/Ingredient] |