Betula occidentalis pollen

Overview

Betula occidentalis pollen is the pollen of the Betula occidentalis plant. Betula 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
Washington/Oregon Inland Tree Mixture	Antigen Laboratories, Inc.	49288-0589	SUBCUTANEOUS, INTRADERMAL	0.0056 g in 1 mL	11/19/2009
Treatment Set TS340826	Antigen Laboratories, Inc.	49288-0812	INTRADERMAL, SUBCUTANEOUS	0.0004 g in 1 mL	3/30/2011
Western 10 Tree Pollen Mix	Greer Laboratories, Inc.	22840-9475	INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS	0.01 g in 1 mL	6/3/2025
Treatment Set TS341824	Antigen Laboratories, Inc.	49288-0818	SUBCUTANEOUS, INTRADERMAL	0.00048 g in 1 mL	6/8/2011
Birch Mixture	Antigen Laboratories, Inc.	49288-0056	SUBCUTANEOUS, INTRADERMAL	0.0083 g in 1 mL	11/19/2009
Washington/Oregon Coastal Tree Mixture	Antigen Laboratories, Inc.	49288-0588	SUBCUTANEOUS, INTRADERMAL	0.0056 g in 1 mL	11/19/2009
Western 10 Tree Pollen Mix	Greer Laboratories, Inc.	22840-9478	INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS	0.005 g in 1 mL	6/3/2025
Birch Mixture	Antigen Laboratories, Inc.	49288-0057	SUBCUTANEOUS, INTRADERMAL	0.0033 g in 1 mL	11/19/2009
Spring (Water) Birch	Antigen Laboratories, Inc.	49288-0058	SUBCUTANEOUS, INTRADERMAL	0.05 g in 1 mL	11/19/2009
Western 10 Tree Pollen Mix	Greer Laboratories, Inc.	22840-9476	INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS	2000 [PNU] in 1 mL	6/3/2025

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
No Health Canada approvals found for this drug.

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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