| NDC Code | 49288-0490-1 |
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| Package Description | 2 mL in 1 VIAL, MULTI-DOSE (49288-0490-1) |
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| Product NDC | 49288-0490 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sunflower Pollen |
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| Non-Proprietary Name | Sunflower Pollen |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRADERMAL; SUBCUTANEOUS |
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| Start Marketing Date | 19740323 |
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| Marketing Category Name | BLA |
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| Application Number | BLA102223 |
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| Manufacturer | Antigen Laboratories, Inc. |
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| Substance Name | HELIANTHUS ANNUUS POLLEN |
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| Strength | .05 |
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| Strength Unit | g/mL |
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| Pharmacy Classes | Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC] |
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