| Product NDC: | 0268-3057 |
| Proprietary Name: | Redtop Grass, Standardized |
| Non Proprietary Name: | Redtop Grass, Standardized |
| Active Ingredient(s): | 100000 [BAU]/mL & nbsp; Redtop Grass, Standardized |
| Administration Route(s): | PERCUTANEOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0268-3057 |
| Labeler Name: | ALK-Abello, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103055 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19971218 |
| Package NDC: | 0268-3057-06 |
| Package Description: | 5 mL in 1 VIAL, MULTI-DOSE (0268-3057-06) |
| NDC Code | 0268-3057-06 |
| Proprietary Name | Redtop Grass, Standardized |
| Package Description | 5 mL in 1 VIAL, MULTI-DOSE (0268-3057-06) |
| Product NDC | 0268-3057 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Redtop Grass, Standardized |
| Dosage Form Name | SOLUTION |
| Route Name | PERCUTANEOUS |
| Start Marketing Date | 19971218 |
| Marketing Category Name | BLA |
| Labeler Name | ALK-Abello, Inc. |
| Substance Name | AGROSTIS GIGANTEA POLLEN |
| Strength Number | 100000 |
| 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] |