Overview
Egg white allergenic 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. | 49288-0188 | SUBCUTANEOUS, INTRADERMAL | 0.05 g in 1 mL | 11/13/2009 | |
| Nelco Laboratories, Inc. | 36987-1131 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/10/2009 | |
| Allergy Laboratories, Inc. | 54575-389 | PERCUTANEOUS, SUBCUTANEOUS | 1 g in 20 mL | 3/15/2011 | |
| Nelco Laboratories, Inc. | 36987-1130 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/10/2009 | |
| Nelco Laboratories, Inc. | 36987-1132 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/10/2009 | |
| Nelco Laboratories, Inc. | 36987-1133 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/10/2009 |
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 |
|---|---|---|---|---|---|
| TRISEQUENS TABLET | SIN06011P | TABLET, FILM COATED | 2 mg | 6/3/1991 |
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 |
|---|---|---|---|---|---|
| ALYSSA TABLETS | N/A | N/A | N/A | 2/7/2025 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| Muscle Builder Tablets | 134847 | Enervite (NSW) Pty Ltd | Medicine | A | 2/12/2007 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| OVI GALLINAE PELLICULA GRANULES 5CH-30CH | dolisos laboratoires s.a. | 00769789 | Tablet - Oral | 3 CH / CH | 12/31/1988 |
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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