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Fusarium oxysporum
Fusarium oxysporum - 49288-0197-5 - (Fusarium oxysporum)
Drug Information of Fusarium oxysporum
| Product NDC: | 49288-0197 |
| Proprietary Name: | Fusarium oxysporum |
| Non Proprietary Name: | Fusarium oxysporum |
| Active Ingredient(s): | .1 g/mL & nbsp; Fusarium oxysporum |
| Administration Route(s): | INTRADERMAL; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fusarium oxysporum
| Product NDC: | 49288-0197 |
| Labeler Name: | Antigen Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA102223 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19740323 |
Package Information of Fusarium oxysporum
| Package NDC: | 49288-0197-5 |
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (49288-0197-5) |
NDC Information of Fusarium oxysporum
| NDC Code | 49288-0197-5 |
| Proprietary Name | Fusarium oxysporum |
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (49288-0197-5) |
| Product NDC | 49288-0197 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fusarium oxysporum |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRADERMAL; SUBCUTANEOUS |
| Start Marketing Date | 19740323 |
| Marketing Category Name | BLA |
| Labeler Name | Antigen Laboratories, Inc. |
| Substance Name | FUSARIUM OXYSPORUM |
| Strength Number | .1 |
| Strength Unit | g/mL |
| Pharmaceutical Classes | Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient] |
