MedPath

Anethole

Generic Name
Anethole
Drug Type
Small Molecule
Chemical Formula
C10H12O
CAS Number
4180-23-8
Unique Ingredient Identifier
Q3JEK5DO4K

Overview

No overview information available.

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
No FDA approvals found for this drug.

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
BRONCO ASMOL
herbes universelles inc.
00365467
Liquid - Oral
1.5 MG / 5 ML
12/31/1966
BENTASIL HONEY-LEMON
carter-horner corp.
02230938
Lozenge - Oral
2.2 MG / LOZ
7/20/1998
BENTASIL GREEN
carter-horner corp.
00691585
Lozenge - Oral
0.01 %
12/31/1987
BEECH NUT MENTHOL COUGH DROP
beta brands limited
02230548
Lozenge - Oral
1.3 MG / LOZ
10/20/1997
BEECH-NUT MENTHOL COUGH DROPS
life savers canada, division of hershey canada inc.
00373494
Lozenge - Oral
1.3 MG / LOZ
12/31/1979
BENTASIL YELLOW
carter-horner corp.
00691593
Lozenge - Oral
.12 % / LOZ
12/31/1981
BENTASIL RED
carter-horner corp.
00514365
Lozenge - Oral
.1 %
12/31/1981
BENTASIL CHERRY
carter-horner corp.
02230937
Lozenge - Oral
2 MG / LOZ
7/20/1998

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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