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Beech Pollen
Beech Pollen - 49643-349-50 - (Fagus grandifolia)
Drug Information of Beech Pollen
| Product NDC: | 49643-349 |
| Proprietary Name: | Beech Pollen |
| Non Proprietary Name: | Fagus grandifolia |
| Active Ingredient(s): | 1 g/20mL & nbsp; Fagus grandifolia |
| Administration Route(s): | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Beech Pollen
| Product NDC: | 49643-349 |
| Labeler Name: | Allermed Laboratories, Inc. |
| Product Type: | NON-STANDARDIZED ALLERGENIC |
| FDA Application Number: | BLA102212 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19740312 |
Package Information of Beech Pollen
| Package NDC: | 49643-349-50 |
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (49643-349-50) |
NDC Information of Beech Pollen
| NDC Code | 49643-349-50 |
| Proprietary Name | Beech Pollen |
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (49643-349-50) |
| Product NDC | 49643-349 |
| Product Type Name | NON-STANDARDIZED ALLERGENIC |
| Non Proprietary Name | Fagus grandifolia |
| Dosage Form Name | INJECTION |
| Route Name | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
| Start Marketing Date | 19740312 |
| Marketing Category Name | BLA |
| Labeler Name | Allermed Laboratories, Inc. |
| Substance Name | FAGUS GRANDIFOLIA 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] |
