Overview
Phoma glomerata is a fungus which can provoke allergic reactions. Phoma glomerata 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. | 36987-2063 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-2060 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-2058 | INTRADERMAL, SUBCUTANEOUS | 20000 [PNU] in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-2055 | INTRADERMAL, SUBCUTANEOUS | 10000 [PNU] in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-2059 | INTRADERMAL, SUBCUTANEOUS | 40000 [PNU] in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-2057 | INTRADERMAL, SUBCUTANEOUS | 20000 [PNU] in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-2056 | INTRADERMAL, SUBCUTANEOUS | 10000 [PNU] in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-2061 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/14/2009 | |
| Nelco Laboratories, Inc. | 36987-2062 | INTRADERMAL, SUBCUTANEOUS | 0.1 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. | |||||
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| No Health Canada approvals found for this drug. | |||||
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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