Agrostis gigantea pollen

Overview

Agrostis gigantea pollen is the pollen of the Agrostis gigantea plant. Agrostis gigantea pollen is mainly 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
Treatment Set TS333938	Antigen Laboratories, Inc.	49288-0657	SUBCUTANEOUS, INTRADERMAL	454.5 [BAU] in 1 mL	12/2/2009
Standardized Redtop Grass Pollen	Nelco Laboratories, Inc.	36987-2364	SUBCUTANEOUS, INTRADERMAL	10000 [BAU] in 1 mL	11/25/2009
STANDARDIZED REDTOP GRASS POLLEN	Allergy Laboratories, Inc.	54575-099	PERCUTANEOUS, SUBCUTANEOUS	100000 [BAU] in 1 mL	3/27/2010
Treatment Set TS128811	Antigen Laboratories, Inc.	49288-0675	SUBCUTANEOUS, INTRADERMAL	1428.6 [BAU] in 1 mL	12/2/2009
Standardized Redtop Grass Pollen	Nelco Laboratories, Inc.	36987-2363	SUBCUTANEOUS, INTRADERMAL	100000 [BAU] in 1 mL	11/25/2009
Treatment Set TS128872	Antigen Laboratories, Inc.	49288-0658	SUBCUTANEOUS, INTRADERMAL	454.5 [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
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product	Company	DIN	Dosage Form	Strength	Market Date
ALLERGENIC EXTRACT - MIXTURE OF 5 STANDARDIZED GRASS POLLEN	alk-abello inc	02325543	Liquid - Subcutaneous , Percutaneous , Intradermal	20000 UNIT / ML	7/30/2009
ALLERGENIC EXTRACTS - 7 GRASS MIX	greer laboratories inc	02425513	Liquid - Subcutaneous	100000 UNIT / ML	6/2/2014
PACIFIC GRASSES & WEED POLLEN VACCINE	bencard allergy laboratories, an allergy therapeutics (canada) ltd. company	00061441	Liquid - Subcutaneous	null NIL / NIL	12/31/1955
ALLERGENIC EXTRACTS, K-O-R-T GRASS MIXTURE	greer laboratories inc	02447231	Solution - Intracutaneous , Subcutaneous	10000 UNIT / ML	N/A
ALLERGENIC EXTRACT - MIXTURE OF 4 STANDARDIZED GRASS POLLEN	alk-abello inc	02325535	Liquid - Intradermal , Percutaneous , Subcutaneous	25000 UNIT / ML	3/22/2011
STANDARDIZED GRASS POLLEN - REDTOP	hollister-stier laboratories llc	02238492	Liquid - Intradermal	100 UNIT / ML	N/A
STANDARDIZED GRASS POLLEN - REDTOP	hollister-stier laboratories llc	02238491	Liquid - Intradermal	1000 UNIT / ML	N/A
ALLERGENIC EXTRACT - STANDARDIZED GRASS POLLEN - RED TOP	greer laboratories inc	02242670	Liquid - Subcutaneous , Intracutaneous	100000 UNIT / ML	10/30/2000
ALLERGENIC EXTRACT - STANDARDIZED REDTOP GRASS POLLEN	alk-abello inc	02325497	Liquid - Subcutaneous , Intradermal , Percutaneous	100000 UNIT / ML	7/30/2009
ALLERGENIC EXTRACTS - 7 GRASS MIX	greer laboratories inc	02425505	Liquid - Subcutaneous	10000 UNIT / ML	9/25/2014

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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