Product NDC: | 0268-0286 |
Proprietary Name: | Redtop Grass, Standardized |
Non Proprietary Name: | Redtop Grass, Standardized |
Active Ingredient(s): | 10000 [BAU]/mL & nbsp; Redtop Grass, Standardized |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0268-0286 |
Labeler Name: | ALK-Abello, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103055 |
Marketing Category: | BLA |
Start Marketing Date: | 19971218 |
Package NDC: | 0268-0286-50 |
Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (0268-0286-50) |
NDC Code | 0268-0286-50 |
Proprietary Name | Redtop Grass, Standardized |
Package Description | 50 mL in 1 VIAL, MULTI-DOSE (0268-0286-50) |
Product NDC | 0268-0286 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Redtop Grass, Standardized |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 19971218 |
Marketing Category Name | BLA |
Labeler Name | ALK-Abello, Inc. |
Substance Name | AGROSTIS GIGANTEA POLLEN |
Strength Number | 10000 |
Strength Unit | [BAU]/mL |
Pharmaceutical Classes | Standardized Pollen Allergenic Extract [EPC],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |