MedPath

Morus alba pollen

Generic Name
Morus alba pollen
Drug Type
Biotech
Unique Ingredient Identifier
3I9T68187H

Overview

Morus alba pollen is the pollen of the Morus alba plant. Morus alba 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.
36987-2800
INTRADERMAL, SUBCUTANEOUS
20000 [PNU] in 1 mL
12/3/2009
Allergy Laboratories, Inc.
54575-947
PERCUTANEOUS, SUBCUTANEOUS
1 g in 20 mL
3/15/2011
Nelco Laboratories, Inc.
36987-2801
INTRADERMAL, SUBCUTANEOUS
40000 [PNU] in 1 mL
12/3/2009
Antigen Laboratories, Inc.
49288-0684
SUBCUTANEOUS, INTRADERMAL
0.002 g in 1 mL
12/2/2009
Antigen Laboratories, Inc.
49288-0657
SUBCUTANEOUS, INTRADERMAL
0.00021 g in 1 mL
12/2/2009
Greer Laboratories, Inc.
22840-9475
INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
0.01 g in 1 mL
6/3/2025
Nelco Laboratories, Inc.
36987-2797
INTRADERMAL, SUBCUTANEOUS
10000 [PNU] in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-2799
INTRADERMAL, SUBCUTANEOUS
20000 [PNU] in 1 mL
12/3/2009
Antigen Laboratories, Inc.
49288-0325
SUBCUTANEOUS, INTRADERMAL
0.05 g in 1 mL
11/19/2009
Antigen Laboratories, Inc.
49288-0691
SUBCUTANEOUS, INTRADERMAL
0.002 g in 1 mL
12/2/2009

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

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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