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 |
|---|---|---|---|---|---|
2024/09/04 | Not Applicable | Completed | |||
2019/01/23 | Phase 2 | Completed | |||
2011/07/19 | Not Applicable | Completed | |||
2010/01/12 | Phase 4 | Completed | |||
2009/12/01 | Phase 4 | Completed | |||
2002/03/25 | Phase 2 | Completed | |||
2002/01/10 | Phase 3 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Newton Laboratories, Inc. | 55714-2596 | ORAL | 6 [hp_X] in 1 mL | 5/21/2025 | |
| Newton Laboratories, Inc. | 55714-4862 | ORAL | 6 [hp_X] in 1 mL | 5/21/2025 | |
| Newton Laboratories, Inc. | 55714-2471 | ORAL | 6 [hp_X] in 1 mL | 9/18/2025 | |
| Newton Laboratories, Inc. | 55714-4748 | ORAL | 6 [hp_X] in 1 mL | 8/20/2025 | |
| Bestmade Natural Products | 82969-6015 | AURICULAR (OTIC) | 30 [hp_C] in 30 [hp_C] | 5/27/2025 | |
| Newton Laboratories, Inc. | 55714-2467 | ORAL | 6 [hp_X] in 1 mL | 8/27/2025 | |
| Bestmade Natural Products | 82969-2066 | ORAL | 30 [hp_C] in 30 [hp_C] | 1/30/2025 | |
| Newton Laboratories, Inc. | 55714-2465 | ORAL | 6 [hp_X] in 1 mL | 8/20/2025 | |
| Newton Laboratories, Inc. | 55714-4297 | ORAL | 6 [hp_X] in 1 mL | 8/6/2025 | |
| Uriel Pharmacy Inc. | 48951-8036 | ORAL | 3 [hp_X] in 1 mL | 9/16/2025 |
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 |
|---|---|---|---|---|---|
| Esberitox Compact | 329784 | Medicine | A | 2/12/2020 | |
| Thompson's Echinacea Complex | 385863 | Medicine | A | 3/18/2022 | |
| Esberitox | 310669 | Medicine | A | 10/23/2018 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| ECHINACEA | nutraceutical corporation | 02241189 | Capsule - Oral | 500 MG / CAP | N/A |
| ECHINACEA ANGUSTIFOLIA GOUTTE 4CH-30CH | dolisos laboratoires s.a. | 00690929 | Drops - Oral | 1 DH / DH | 12/31/1987 |
| ECHINACEE | santé naturelle (ag) ltée | 02239424 | Capsule - Oral | 1000 MG | 3/19/1999 |
| BELLADONNA HOMACCORD HEEL-021 DPS | 01968858 | Drops - Oral | 1.5 ML / 100 ML | 12/31/1992 | |
| THYMUS AND ECHINACEA NF | nf formulas inc. | 00729590 | Drops - Oral | 3 X / X | 12/31/1988 |
| I.M. AID CAPLETS | nu-life nutrition ltd. | 00757926 | Tablet - Oral | 16.67 MG | 12/31/1988 |
| TRAUMEEL HEEL-082 TAB | 01969498 | Tablet - Oral | 2 DH / TAB | 12/31/1992 | |
| ECHINACEA PWR 3X | koegler laboratories inc. | 00867721 | Powder - Oral | 3 X / X | 12/31/1989 |
| ECHINACEA CAPSULES 400MG | mczand herbal inc. | 02131390 | Capsule - Oral | 400 MG / CAP | 12/31/1995 |
| ECHINACEA ROOT EXTRACT LOZENGES | ashbury research corporation | 02239369 | Lozenge - Oral | 500 MG / LOZ | N/A |
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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