NDC Code | 49288-0020-1 |
Package Description | 2 mL in 1 VIAL, MULTI-DOSE (49288-0020-1) |
Product NDC | 49288-0020 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Oregon Ash |
Non-Proprietary Name | Oregon Ash |
Dosage Form | INJECTION, SOLUTION |
Usage | INTRADERMAL; SUBCUTANEOUS |
Start Marketing Date | 19740423 |
Marketing Category Name | BLA |
Application Number | BLA102223 |
Manufacturer | Antigen Laboratories, Inc. |
Substance Name | FRAXINUS LATIFOLIA POLLEN |
Strength | .05 |
Strength Unit | g/mL |
Pharmacy Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS] |