NDC Code | 54575-169-30 |
Package Description | 30 mL in 1 VIAL, MULTI-DOSE (54575-169-30) |
Product NDC | 54575-169 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Dock Mix, Sour Sheep Sorrel/yellow Pollen |
Non-Proprietary Name | Rumex Acetosella Pollen And Rumex Crispus Pollen |
Dosage Form | INJECTION, SOLUTION |
Usage | PERCUTANEOUS; SUBCUTANEOUS |
Start Marketing Date | 19671207 |
Marketing Category Name | BLA |
Application Number | BLA101376 |
Manufacturer | Allergy Laboratories, Inc. |
Substance Name | RUMEX ACETOSELLA POLLEN; RUMEX CRISPUS POLLEN |
Strength | .5; .5 |
Strength Unit | g/20mL; g/20mL |
Pharmacy Classes | Non-Standardized Pollen Allergenic Extract [EPC],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Increased Histamine Release [PE],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS] |