MedPath

Hordeum vulgare pollen

Generic Name
Hordeum vulgare pollen
Drug Type
Biotech
Unique Ingredient Identifier
2LN3M29LNI

Overview

Hordeum vulgare pollen is the pollen of the Hordeum vulgare plant. Hordeum vulgare 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
Allergy Laboratories, Inc.
54575-082
PERCUTANEOUS, SUBCUTANEOUS
1 g in 20 mL
3/15/2011

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
AN SHEN DING ZHI WAN
483345
Medicine
A
3/20/2025
AN SHEN DING ZHI WAN
495112
Medicine
A
6/30/2025
LIVE TONIC VITAMIN B COMPLEX
148298
Medicine
A
12/10/2007
Kids Multi
329564
Medicine
A
2/6/2020
An Shen Ding Zhi Wan -(Zizyphus & Polygala Formula)
351524
Medicine
A
12/10/2020
Super Mushrooms and Greens
449618
Medicine
A
5/24/2024
Bao He Xiao Shi Fang a.k.a Citrus & Crataegus Digest-Aid Formula
110616
Medicine
A
9/30/2004
PM Essentials
342492
Regulatory Services Australia
Medicine
A
8/27/2020
MSM Alive
217766
Pharma Botanica Pty Ltd
Medicine
A
11/26/2013
Men's Multi
324309
Medicine
A
10/1/2019

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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