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 |
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No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
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No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
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No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
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No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
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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 |
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No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
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No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
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No UK EMC drug information found for this drug. |
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