| NDC Code | 49643-309-50 |
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| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (49643-309-50) |
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| Product NDC | 49643-309 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Standardized Redtop Grass |
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| Non-Proprietary Name | Agrostis Alba |
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| Dosage Form | INJECTION |
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| Usage | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
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| Start Marketing Date | 19961202 |
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| Marketing Category Name | BLA |
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| Application Number | BLA102218 |
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| Manufacturer | Allermed Laboratories, Inc. |
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| Substance Name | AGROSTIS GIGANTEA POLLEN |
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| Strength | 100000 |
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| Strength Unit | [BAU]/mL |
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| Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS], Standardized Pollen Allergenic Extract [EPC] |
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