Overview
Vespula vulgaris venom protein is an extract of Vespula vulgaris venom. Vespula vulgaris venom protein 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 |
|---|---|---|---|---|---|
| Bestmade Natural Products | 82969-2054 | ORAL | 100 [hp_C] in 100 [hp_C] | 1/24/2025 |
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 |
|---|---|---|---|---|---|
| VENOMIL YELLOW JACKET VENOM PROTEIN (120MCG) | 02226286 | Powder For Solution - Subcutaneous
,
Intradermal | 120 MCG / VIAL | 8/28/1998 | |
| HYMENOPTERA VENOM PRODUCT - YELLOW JACKET VENOM PROTEIN (550 MCG) | 02220113 | Powder For Solution - Subcutaneous | 550 MCG / VIAL | 12/16/1997 | |
| HYMENOPTERA VENOM PRODUCT-MIXED VESPID VENOM PROTEIN (1650 MCG) | 02221314 | Powder For Solution - Subcutaneous | 550 MCG / VIAL | 12/16/1997 | |
| VENOMIL YELLOW JACKET VENOM PROTEIN (12MCG) | hollister-stier laboratories llc | 02226278 | Kit
,
Powder For Solution - Intradermal | 12 MCG / VIAL | 9/15/1998 |
| VENOMIL MIXED VESPID VENOM PROTEIN (360MCG) | 02226294 | Powder For Solution - Subcutaneous
,
Intradermal | 120 MCG / VIAL | 8/28/1998 | |
| YELLOW JACKET VENOM PROTEIN INJ | hollister-stier, unit pharm, division of miles canada inc. | 00499633 | Powder For Solution - Subcutaneous
,
Intradermal | 500 MCG / VIAL | 12/31/1980 |
| PHARMALGEN MIXED VESPID VENOM PROTEIN | 01948873 | Powder For Solution - Subcutaneous
,
Intradermal | 1.1 MG / VIAL | 12/31/1992 | |
| MIXED VESPID VENOM PROTEIN INJ | hollister-stier, unit pharm, division of miles canada inc. | 00583448 | Powder For Solution - Subcutaneous | 550 MCG / VIAL | 12/31/1983 |
| VENOMIL INJ 10MCG/ML YELLOW JACKET | hollister-stier, unit pharm, division of miles canada inc. | 00605298 | Liquid - Subcutaneous | 10 MCG / ML | 12/31/1983 |
| VENOMIL INJ MIXED 300MCG/DOSE | hollister-stier, unit pharm, division of miles canada inc. | 00602809 | Liquid - Subcutaneous | 100 MCG / ML | 12/31/1983 |
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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