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SUNFLOWER POLLEN
SUNFLOWER POLLEN - 54575-179-50 - (helianthus annuus pollen)
Drug Information of SUNFLOWER POLLEN
| Product NDC: | 54575-179 |
| Proprietary Name: | SUNFLOWER POLLEN |
| Non Proprietary Name: | helianthus annuus pollen |
| Active Ingredient(s): | 1 g/20mL & nbsp; helianthus annuus pollen |
| Administration Route(s): | PERCUTANEOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUNFLOWER POLLEN
| Product NDC: | 54575-179 |
| Labeler Name: | Allergy Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA101376 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19671207 |
Package Information of SUNFLOWER POLLEN
| Package NDC: | 54575-179-50 |
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (54575-179-50) |
NDC Information of SUNFLOWER POLLEN
| NDC Code | 54575-179-50 |
| Proprietary Name | SUNFLOWER POLLEN |
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (54575-179-50) |
| Product NDC | 54575-179 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | helianthus annuus pollen |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | PERCUTANEOUS; SUBCUTANEOUS |
| Start Marketing Date | 19671207 |
| Marketing Category Name | BLA |
| Labeler Name | Allergy Laboratories, Inc. |
| Substance Name | HELIANTHUS ANNUUS POLLEN |
| Strength Number | 1 |
| Strength Unit | g/20mL |
| Pharmaceutical Classes | Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |
