Overview
Eurotium herbariorum is a fungus which can provoke allergic reactions. Eurotium herbariorum extract is used in allergenic testing.
Background
Eurotium herbariorum is a fungus which can provoke allergic reactions. Eurotium herbariorum extract is used in allergenic testing.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|
No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Nelco Laboratories, Inc. | 36987-1881 | SUBCUTANEOUS, INTRADERMAL | 0.05 g in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-1878 | SUBCUTANEOUS, INTRADERMAL | 20000 [PNU] in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-1876 | SUBCUTANEOUS, INTRADERMAL | 10000 [PNU] in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-1883 | SUBCUTANEOUS, INTRADERMAL | 0.1 g in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-1882 | SUBCUTANEOUS, INTRADERMAL | 0.1 g in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-1879 | SUBCUTANEOUS, INTRADERMAL | 40000 [PNU] in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-1875 | SUBCUTANEOUS, INTRADERMAL | 10000 [PNU] in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-1877 | SUBCUTANEOUS, INTRADERMAL | 20000 [PNU] in 1 mL | 12/14/2009 | |
| Allergy Laboratories, Inc. | 54575-183 | PERCUTANEOUS, SUBCUTANEOUS | 1 g in 20 mL | 3/15/2011 | |
| Nelco Laboratories, Inc. | 36987-1880 | SUBCUTANEOUS, INTRADERMAL | 0.05 g in 1 mL | 12/14/2009 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No HSA approvals found for this drug. | |||||
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| No TGA approvals found for this drug. | |||||