Overview
Cynodon dactylon pollen, also known as bermuda grass pollen, is a standardized grass pollen extracts used for the diagnosis and treatment of allergic disease to grass pollen. It can be cutaneously, intradermally and subcutaneously administered to initiate an immune response in case of an allergic reaction. Diagnostic allergenic extracts are primarily indicated for establishing clinical relevance of specific allergens to which the patient has been exposed and the degree of sensitivity the patient has toward that allergen.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
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No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
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Antigen Laboratories, Inc. | 49288-0854 | SUBCUTANEOUS, INTRADERMAL | 1000 [BAU] in 1 mL | 5/11/2012 | |
Antigen Laboratories, Inc. | 49288-0772 | SUBCUTANEOUS, INTRADERMAL | 16 [BAU] in 1 mL | 12/2/2009 | |
Antigen Laboratories, Inc. | 49288-0797 | SUBCUTANEOUS, INTRADERMAL | 80 [BAU] in 1 mL | 12/1/2010 | |
Antigen Laboratories, Inc. | 49288-0801 | SUBCUTANEOUS, INTRADERMAL | 400 [BAU] in 1 mL | 1/13/2011 | |
Nelco Laboratories, Inc. | 36987-2270 | INTRADERMAL, SUBCUTANEOUS | 10000 [BAU] in 1 mL | 11/25/2009 | |
Antigen Laboratories, Inc. | 49288-0846 | SUBCUTANEOUS, INTRADERMAL | 400 [BAU] in 1 mL | 3/23/2012 | |
Antigen Laboratories, Inc. | 49288-0849 | SUBCUTANEOUS, INTRADERMAL | 1000 [BAU] in 1 mL | 5/11/2012 | |
Antigen Laboratories, Inc. | 49288-0718 | SUBCUTANEOUS, INTRADERMAL | 400 [BAU] in 1 mL | 12/2/2009 | |
Antigen Laboratories, Inc. | 49288-0786 | SUBCUTANEOUS, INTRADERMAL | 16 [BAU] in 1 mL | 6/17/2010 | |
Antigen Laboratories, Inc. | 49288-0708 | SUBCUTANEOUS, INTRADERMAL | 333.33 [BAU] in 1 mL | 12/2/2009 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
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No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
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No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
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SOUTHERN GRASS MIX (1:20) Scratch test & treatment | 32705 | Medicine | A | 11/1/1991 | |
BERMUDA GRASS (1:20) Scratch test & treatment | 32658 | Medicine | A | 11/1/1991 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
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ALLERGENIC EXTRACT - STANDARDIZED GRASS POLLEN - BERMUDA | greer laboratories inc | 02242663 | Liquid - Subcutaneous
,
Intracutaneous | 10000 UNIT / ML | 3/26/2001 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
TUTUKON SOLUCION ORAL | Setonda S.L. | 82648 | SOLUCIÓN ORAL | Sin Receta | Commercialized |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
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No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
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No UK EMC drug information found for this drug. |
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