MedPath

Betula occidentalis pollen

Generic Name
Betula occidentalis pollen
Drug Type
Biotech
Unique Ingredient Identifier
R889N2L976

Overview

Betula occidentalis pollen is the pollen of the Betula occidentalis plant. Betula occidentalis pollen is mainly used in allergenic testing.

Background

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 Approved Products

Product Name
Manufacturer
Route
Strength
Approved
NDC Code
SUBCUTANEOUS, INTRADERMAL
0.05 g in 1 mL
2009/11/19
49288-0058
SUBCUTANEOUS, INTRADERMAL
0.00048 g in 1 mL
2011/06/08
49288-0818
SUBCUTANEOUS, INTRADERMAL
0.0033 g in 1 mL
2009/11/19
49288-0057
SUBCUTANEOUS, INTRADERMAL
0.0056 g in 1 mL
2009/11/19
49288-0589
SUBCUTANEOUS, INTRADERMAL
0.0056 g in 1 mL
2009/11/19
49288-0588
INTRADERMAL, SUBCUTANEOUS
0.0004 g in 1 mL
2011/03/30
49288-0812
SUBCUTANEOUS, INTRADERMAL
0.0083 g in 1 mL
2009/11/19
49288-0056

EMA Approved Products

Medicine Name
EMA Number
Auth. Holder
Country
Drug Type
Status
Issued
Opinion
Revision

No EMA products found

No EMA products found for this drug

HSA Approved Products

Product Name
Manufacturer
Dosage Form
Strength
Approved
Approval No.

No HSA products found

No HSA products found for this drug

NMPA Approved Products

Product Name
Approval No.
Manufacturer
Dosage Form
Trade Name
Strength
Type
Status
Date
Import

No NMPA products found

No NMPA products found for this drug

PPB Approved Products

Product Name
Registration Code
Company
Category
Sale Type
Reg. Date

No PPB products found

No PPB products found for this drug

TGA Approved Products

Product Name
ARTG ID
Sponsor
Status
Reg. Date
Ingredient

No TGA products found

No TGA products found for this drug

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