MedPath

Quercus agrifolia pollen

Generic Name
Quercus agrifolia pollen
Drug Type
Biotech
Unique Ingredient Identifier
VOT5MA71M7

Overview

Quercus agrifolia pollen is the pollen of the Quercus agrifolia plant. Quercus agrifolia pollen is mainly used in allergenic testing.

Background

Quercus agrifolia pollen is the pollen of the Quercus agrifolia plant. Quercus agrifolia 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
Nelco Laboratories, Inc.
36987-2848
INTRADERMAL, SUBCUTANEOUS
20000 [PNU] in 1 mL
12/3/2009
Greer Laboratories, Inc.
22840-9472
SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS
0.0166666 g in 1 mL
6/3/2025
Nelco Laboratories, Inc.
36987-2851
INTRADERMAL, SUBCUTANEOUS
0.05 g in 1 mL
12/3/2009
Greer Laboratories, Inc.
22840-9469
SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS
0.0333333 g in 1 mL
6/3/2025
Antigen Laboratories, Inc.
49288-0337
SUBCUTANEOUS, INTRADERMAL
0.05 g in 1 mL
11/19/2009
Greer Laboratories, Inc.
22840-9805
SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS
0.0166666 g in 1 mL
6/3/2025
Greer Laboratories, Inc.
22840-9806
INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
6666.6666 [PNU] in 1 mL
6/3/2025
Nelco Laboratories, Inc.
36987-2849
INTRADERMAL, SUBCUTANEOUS
40000 [PNU] in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-2850
INTRADERMAL, SUBCUTANEOUS
0.05 g in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-2847
INTRADERMAL, SUBCUTANEOUS
20000 [PNU] in 1 mL
12/3/2009

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.
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