Overview
Alternaria alternata is a fungus which can provoke allergic reactions. Alternaria alternata 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 |
|---|---|---|---|---|---|
| Antigen Laboratories, Inc. | 49288-0762 | SUBCUTANEOUS, INTRADERMAL | 0.00008 g in 1 mL | 12/2/2009 | |
| Antigen Laboratories, Inc. | 49288-0210 | SUBCUTANEOUS, INTRADERMAL | 0.0125 g in 1 mL | 11/17/2009 | |
| Antigen Laboratories, Inc. | 49288-0849 | SUBCUTANEOUS, INTRADERMAL | 0.002 g in 1 mL | 5/11/2012 | |
| Antigen Laboratories, Inc. | 49288-0831 | SUBCUTANEOUS, INTRADERMAL | 0.01 g in 1 mL | 12/29/2011 | |
| Nelco Laboratories, Inc. | 36987-1857 | INTRADERMAL, SUBCUTANEOUS | 10000 [PNU] in 1 mL | 12/14/2009 | |
| Antigen Laboratories, Inc. | 49288-0786 | SUBCUTANEOUS, INTRADERMAL | 0.002 g in 1 mL | 6/17/2010 | |
| Antigen Laboratories, Inc. | 49288-0842 | SUBCUTANEOUS, INTRADERMAL | 0.002 g in 1 mL | 3/23/2012 | |
| Antigen Laboratories, Inc. | 49288-0708 | SUBCUTANEOUS, INTRADERMAL | 0.00017 g in 1 mL | 12/2/2009 | |
| Antigen Laboratories, Inc. | 49288-0704 | SUBCUTANEOUS, INTRADERMAL | 0.00017 g in 1 mL | 12/2/2009 | |
| Antigen Laboratories, Inc. | 49288-0765 | SUBCUTANEOUS, INTRADERMAL | 0.002 g in 1 mL | 12/2/2009 |
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 |
|---|---|---|---|---|---|
| ALTERNARIA TENUIS (1:10) Scratch test & treatment | 32618 | Medicine | A | 11/1/1991 | |
| Test | 32704 | Medicine | A | 11/1/1991 |
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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