| NDC Code | 54575-169-50 |
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| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (54575-169-50) |
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| Product NDC | 54575-169 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dock Mix, Sour Sheep Sorrel/yellow Pollen |
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| Non-Proprietary Name | Rumex Acetosella Pollen And Rumex Crispus Pollen |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | PERCUTANEOUS; SUBCUTANEOUS |
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| Start Marketing Date | 19671207 |
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| Marketing Category Name | BLA |
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| Application Number | BLA101376 |
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| Manufacturer | Allergy Laboratories, Inc. |
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| Substance Name | RUMEX ACETOSELLA POLLEN; RUMEX CRISPUS POLLEN |
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| Strength | .5; .5 |
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| Strength Unit | g/20mL; g/20mL |
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| Pharmacy Classes | Non-Standardized Pollen Allergenic Extract [EPC],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Increased Histamine Release [PE],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS] |
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