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 |
|---|---|---|---|---|---|
| Newton Laboratories, Inc. | 55714-4298 | ORAL | 15 [hp_X] in 1 mL | 9/8/2025 | |
| King Bio Inc. | 57955-4809 | ORAL | 12 [hp_X] in 118 mL | 5/2/2025 |
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 |
|---|---|---|---|---|---|
| Hayfever Oral Spray | 351128 | Medicine | A | 12/8/2020 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| MEDIPLEX 600 - LIQ | mediherb inc. | 02116928 | Liquid - Oral | 10 X / ML | 12/19/1996 |
| TOBTOX | bio active canada ltd. | 02233688 | Liquid - Oral | 12 X | 5/26/1998 |
| NAPHTALINUM | dolisos canada inc. | 02234621 | Liquid
,
Granules
,
Globules - Oral | 3 X | 1/5/1998 |
| NAPHTALINUM - (3CH-30CH) TAB | homeocan inc. | 02108291 | Tablet - Oral | 3 CH / TAB | 12/31/1994 |
| NAPHTALINUM GOUTTE 1CH - 30CH | boiron laboratoires | 00671126 | Drops - Oral | 1 CH / CH | 12/31/1987 |
| NAPHTALINUM GRANULE 3CH - 30CH | dolisos laboratoires s.a. | 00698679 | Tablet - Oral | 3 CH / CH | 12/31/1987 |
| NAPTHALIN-INJEEL FORTE LIQ (6D,12D,30D,200D/1.1ML) | 02052318 | Liquid - Oral | 6 D / 1.1 ML | 12/31/1993 | |
| NAPHTHALINUM | homeocan inc. | 02234052 | Granules
,
Drops
,
Globules - Oral | 3 X | 1/29/1998 |
| NAPHTALINUM GLOBULE 1CH - 30CH | boiron laboratoires | 00670464 | Tablet - Oral | 1 CH / CH | 12/31/1986 |
| NAPHTALINUM GRANULE 1CH | homeocan inc. | 00859265 | Tablet - Oral | 1 CH / CH | 12/31/1989 |
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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