NDC Code |
49288-0454-5 |
Proprietary Name |
Short/Giant Ragweed Mixture |
Package Description |
50 mL in 1 VIAL, MULTI-DOSE (49288-0454-5) |
Product NDC |
49288-0454 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Short/Giant Ragweed Mixture |
Dosage Form Name |
INJECTION, SOLUTION |
Route Name |
INTRADERMAL; SUBCUTANEOUS |
Start Marketing Date |
19740323 |
Marketing Category Name |
BLA |
Labeler Name |
Antigen Laboratories, Inc. |
Substance Name |
AMBROSIA ARTEMISIIFOLIA POLLEN; AMBROSIA TRIFIDA POLLEN |
Strength Number |
.025; .025 |
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] |