MedPath

Festuca pratensis pollen

Generic Name
Festuca pratensis pollen
Drug Type
Biotech
Unique Ingredient Identifier
IOL9HH67Y9

Overview

Festuca pratensis pollen is the pollen of the Festuca pratensis plant. Festuca pratensis 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.
36987-2319
SUBCUTANEOUS, INTRADERMAL
100000 [BAU] in 1 mL
11/25/2009
Antigen Laboratories, Inc.
49288-0812
INTRADERMAL, SUBCUTANEOUS
4761.9 [BAU] in 1 mL
3/30/2011
Antigen Laboratories, Inc.
49288-0657
SUBCUTANEOUS, INTRADERMAL
454.5 [BAU] in 1 mL
12/2/2009
Antigen Laboratories, Inc.
49288-0802
SUBCUTANEOUS, INTRADERMAL
4000 [BAU] in 1 mL
3/15/2011
Allergy Laboratories, Inc.
54575-092
PERCUTANEOUS, SUBCUTANEOUS
100000 [BAU] in 1 mL
3/27/2010
Antigen Laboratories, Inc.
49288-0827
INTRADERMAL, SUBCUTANEOUS
800 [BAU] in 1 mL
11/22/2011
Antigen Laboratories, Inc.
49288-0725
SUBCUTANEOUS, INTRADERMAL
800 [BAU] in 1 mL
12/2/2009
Antigen Laboratories, Inc.
49288-0675
SUBCUTANEOUS, INTRADERMAL
1428.6 [BAU] in 1 mL
12/2/2009
Antigen Laboratories, Inc.
49288-0834
INTRADERMAL, SUBCUTANEOUS
400 [BAU] in 1 mL
12/29/2011
Antigen Laboratories, Inc.
49288-0851
INTRADERMAL, SUBCUTANEOUS
800 [BAU] in 1 mL
5/11/2012

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
STANDARDIZED GRASS POLLEN - MEADOW FESCUE (1000 BAU/ML)
hollister-stier laboratories llc
02238474
Liquid - Intradermal
1000 UNIT / ML
N/A
STANDARDIZED GRASS POLLEN - MEADOW FESCUE (10000 BAU/ML)
02238473
Solution - Percutaneous ,  Subcutaneous
10000 UNIT / ML
4/11/2001
STANDARDIZED GRASS POLLEN - MEADOW FESCUE (100000 BAU/ML)
02238472
Solution - Percutaneous ,  Subcutaneous
100000 UNIT / ML
10/3/2000
ALLERGENIC EXTRACTS - 7 GRASS MIX
greer laboratories inc
02425513
Liquid - Subcutaneous
100000 UNIT / ML
6/2/2014
ALLERGENIC EXTRACT - STANDARDIZED MEADOW FESCUE GRASS POLLEN
alk-abello inc
02325527
Liquid - Intradermal ,  Subcutaneous ,  Percutaneous
100000 UNIT / ML
7/30/2009
ALLERGENIC EXTRACT - STANDARDIZED GRASS POLLEN - MEADOW FESCUE
greer laboratories inc
02242673
Liquid - Intracutaneous ,  Subcutaneous
10000 UNIT / ML
N/A
STANDARDIZED GRASS POLLEN - MEADOW FESCUE (100 BAU/ML)
hollister-stier laboratories llc
02238475
Liquid - Intradermal
100 UNIT / ML
N/A
ALLERGENIC EXTRACT - STANDARDIZED GRASS POLLEN - MEADOW FESCUE
greer laboratories inc
02242672
Liquid - Subcutaneous ,  Intracutaneous
100000 UNIT / ML
10/30/2000
ALLERGENIC EXTRACTS - 7 GRASS MIX
greer laboratories inc
02425505
Liquid - Subcutaneous
10000 UNIT / ML
9/25/2014

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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