MedPath

Buckwheat

Generic Name
Buckwheat
Drug Type
Biotech
Unique Ingredient Identifier
N0Y68724R3

Overview

Buckwheat allergenic extract is used in allergenic testing.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Clinical Trials

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Nelco Laboratories, Inc.
36987-1566
INTRADERMAL, SUBCUTANEOUS
0.05 g in 1 mL
12/9/2009
Nelco Laboratories, Inc.
36987-1568
INTRADERMAL, SUBCUTANEOUS
0.1 g in 1 mL
12/9/2009
Antigen Laboratories, Inc.
49288-0051
SUBCUTANEOUS, INTRADERMAL
0.05 g in 1 mL
11/17/2009
Allergy Laboratories, Inc.
54575-358
PERCUTANEOUS, SUBCUTANEOUS
1 g in 20 mL
3/15/2011
Bispit Canada Ltd.
85631-003
ORAL
91 mg in 1.3 g
8/2/2025
Nelco Laboratories, Inc.
36987-1567
INTRADERMAL, SUBCUTANEOUS
0.05 g in 1 mL
12/9/2009
Nelco Laboratories, Inc.
36987-1569
INTRADERMAL, SUBCUTANEOUS
0.1 g in 1 mL
12/9/2009

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.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
FAGOPYRUM ESCULENTUM
dolisos canada inc.
02234480
Globules ,  Liquid ,  Granules - Oral
1 X
1/5/1998
BOROPLEX
bio active canada ltd.
02233591
Liquid - Oral
1 X
5/26/1998
FAGOPYRUM-INJEEL LIQ (12D,30D,200D/1.1ML)
02062992
Liquid - Oral
12 D / 1.1 ML
12/31/1994
FAGOPYRUM-INJEEL FORTE LIQ (4D,12D,30D,200D/1.1ML)
02063018
Liquid - Oral
4 D / 1.1 ML
12/31/1994
HOMEOPATHIC MEDICINE (S#740) DPS 30C
total health centre
02082969
Drops - Oral
30 C / ML
12/31/1994
UNDA 245
seroyal international inc.
02233243
Liquid ,  Pellet ,  Tablet ,  Granules ,  Drops - Oral
4 X
4/6/1998
VERMEX
bio active canada ltd.
02233697
Liquid - Oral
3 X
5/26/1998
EQUISTAPLEX
bio active canada ltd.
02233610
Liquid - Oral
1 X
5/26/1998
FAGOPYRUM ESCULANTUM GRANULES 1DH-30CH
dolisos laboratoires s.a.
00768545
Tablet - Oral
1 DH / DH
12/31/1988

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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