MedPath

Cynodon dactylon pollen

Generic Name
Cynodon dactylon pollen
Drug Type
Biotech
Unique Ingredient Identifier
2Q8MR21NHK

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

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.
49288-0854
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
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
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
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
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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