MedPath

Juniperus occidentalis pollen

Generic Name
Juniperus occidentalis pollen
Drug Type
Biotech
Unique Ingredient Identifier
7JWJ3HXZ9U

Overview

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

Background

Juniperus occidentalis pollen is the pollen of the Juniperus occidentalis plant. Juniperus 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
Greer Laboratories, Inc.
22840-9475
INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
0.01 g in 1 mL
6/3/2025
Nelco Laboratories, Inc.
36987-2717
INTRADERMAL, SUBCUTANEOUS
10000 [PNU] in 1 mL
12/3/2009
Antigen Laboratories, Inc.
49288-0281
SUBCUTANEOUS, INTRADERMAL
0.05 g in 1 mL
11/19/2009
Nelco Laboratories, Inc.
36987-2723
INTRADERMAL, SUBCUTANEOUS
0.05 g in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-2718
INTRADERMAL, SUBCUTANEOUS
10000 [PNU] in 1 mL
12/3/2009
Greer Laboratories, Inc.
22840-9478
INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS
0.005 g in 1 mL
6/3/2025
Nelco Laboratories, Inc.
36987-2724
INTRADERMAL, SUBCUTANEOUS
0.1 g in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-2719
INTRADERMAL, SUBCUTANEOUS
20000 [PNU] in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-2720
INTRADERMAL, SUBCUTANEOUS
20000 [PNU] in 1 mL
12/3/2009
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.
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