Platanus occidentalis pollen

Overview

Platanus occidentalis pollen is the pollen of the Platanus occidentalis plant. Platanus occidentalis 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 TS340826	Antigen Laboratories, Inc.	49288-0812	INTRADERMAL, SUBCUTANEOUS	0.0024 g in 1 mL	3/30/2011
East Sycamore	Nelco Laboratories, Inc.	36987-3047	INTRADERMAL, SUBCUTANEOUS	20000 [PNU] in 1 mL	12/3/2009
Treatment Set TS331046	Antigen Laboratories, Inc.	49288-0704	SUBCUTANEOUS, INTRADERMAL	0.0017 g in 1 mL	12/2/2009
Eastern 10 Tree Pollen Mix	Greer Laboratories, Inc.	22840-9465	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS	0.005 g in 1 mL	6/3/2025
Treatment Set TS330317	Antigen Laboratories, Inc.	49288-0684	SUBCUTANEOUS, INTRADERMAL	0.002 g in 1 mL	12/2/2009
11 Tree Pollen Mix	Greer Laboratories, Inc.	22840-9484	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS	0.0045454 g in 1 mL	6/3/2025
Treatment Set TS333938	Antigen Laboratories, Inc.	49288-0657	SUBCUTANEOUS, INTRADERMAL	0.00021 g in 1 mL	12/2/2009
Treatment Set TS333312	Antigen Laboratories, Inc.	49288-0667	INTRADERMAL, SUBCUTANEOUS	0.01 g in 1 mL	12/2/2009
11 Tree Pollen Mix	Greer Laboratories, Inc.	22840-9482	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS	1818.1818 [PNU] in 1 mL	6/3/2025
Treatment Set TS337681	Antigen Laboratories, Inc.	49288-0793	SUBCUTANEOUS, INTRADERMAL	0.0016666 g in 1 mL	10/13/2010

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
AMERICAN SYCAMORE (1:20) Scratch test & treatment	32663	Stallergenes Australia Pty Ltd	Medicine	A	11/1/1991

Health Canada Drug Approvals

Approved Product	Company	DIN	Dosage Form	Strength	Market Date
DIATHESIS IV	bio active canada ltd.	02233601	Liquid - Oral	12 X	5/26/1998
PLATANUS	dolisos canada inc.	02234672	Liquid , Granules , Globules - Oral	1 X	1/5/1998
HDR I	bio active canada ltd.	02233622	Liquid - Oral	12 X	5/26/1998
CANDOPT	terra botanica products ltd.	02233305	Liquid - Oral	12 X	5/25/1998
CANDNIX HP	terra botanica products ltd.	02233304	Liquid - Oral	12 X	5/25/1998
PSORI-BOSAN B77	professional health products	02232196	Ointment - Topical	1 D	4/1/1998
COSMETOPT	terra botanica products ltd.	02233311	Liquid - Oral	12 X	5/25/1998
PLATANUS ORIENTALIS	seroyal international inc.	02233194	Globules , Tablet , Pellet , Granules , Drops , Liquid - Oral	1 X	4/6/1998

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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