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SPONDYLOCLADIUM ATROVIRENS
SPONDYLOCLADIUM ATROVIRENS - 54575-220-30 - (helminthosporium solani)
Drug Information of SPONDYLOCLADIUM ATROVIRENS
| Product NDC: | 54575-220 |
| Proprietary Name: | SPONDYLOCLADIUM ATROVIRENS |
| Non Proprietary Name: | helminthosporium solani |
| Active Ingredient(s): | 1 g/20mL & nbsp; helminthosporium solani |
| Administration Route(s): | PERCUTANEOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SPONDYLOCLADIUM ATROVIRENS
| Product NDC: | 54575-220 |
| Labeler Name: | Allergy Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA101376 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19671207 |
Package Information of SPONDYLOCLADIUM ATROVIRENS
| Package NDC: | 54575-220-30 |
| Package Description: | 30 mL in 1 VIAL, MULTI-DOSE (54575-220-30) |
NDC Information of SPONDYLOCLADIUM ATROVIRENS
| NDC Code | 54575-220-30 |
| Proprietary Name | SPONDYLOCLADIUM ATROVIRENS |
| Package Description | 30 mL in 1 VIAL, MULTI-DOSE (54575-220-30) |
| Product NDC | 54575-220 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | helminthosporium solani |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | PERCUTANEOUS; SUBCUTANEOUS |
| Start Marketing Date | 19671207 |
| Marketing Category Name | BLA |
| Labeler Name | Allergy Laboratories, Inc. |
| Substance Name | HELMINTHOSPORIUM SOLANI |
| Strength Number | 1 |
| Strength Unit | g/20mL |
| 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] |
