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Short Ragweed
Short Ragweed - 49643-315-50 - (Ambrosia artemisiifolia)
Drug Information of Short Ragweed
| Product NDC: | 49643-315 |
| Proprietary Name: | Short Ragweed |
| Non Proprietary Name: | Ambrosia artemisiifolia |
| Active Ingredient(s): | 1 g/10mL & nbsp; Ambrosia artemisiifolia |
| Administration Route(s): | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Short Ragweed
| Product NDC: | 49643-315 |
| Labeler Name: | Allermed Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103118 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19820101 |
Package Information of Short Ragweed
| Package NDC: | 49643-315-50 |
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (49643-315-50) |
NDC Information of Short Ragweed
| NDC Code | 49643-315-50 |
| Proprietary Name | Short Ragweed |
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (49643-315-50) |
| Product NDC | 49643-315 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ambrosia artemisiifolia |
| Dosage Form Name | INJECTION |
| Route Name | CUTANEOUS; INTRADERMAL; SUBCUTANEOUS |
| Start Marketing Date | 19820101 |
| Marketing Category Name | BLA |
| Labeler Name | Allermed Laboratories, Inc. |
| Substance Name | AMBROSIA ARTEMISIIFOLIA POLLEN |
| Strength Number | 1 |
| Strength Unit | g/10mL |
| Pharmaceutical Classes | Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient] |
