Overview
Thyme allergenic extract is used in allergenic testing.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2023/06/02 | Phase 3 | Active, not recruiting | |||
2023/05/16 | Phase 4 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Allergy Laboratories, Inc. | 54575-465 | PERCUTANEOUS, SUBCUTANEOUS | 1 g in 20 mL | 3/15/2011 | |
| Nelco Laboratories, Inc. | 36987-1747 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/9/2009 | |
| Nelco Laboratories, Inc. | 36987-1746 | INTRADERMAL, SUBCUTANEOUS | 0.05 g in 1 mL | 12/9/2009 | |
| Nelco Laboratories, Inc. | 36987-1749 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/9/2009 | |
| Nelco Laboratories, Inc. | 36987-1748 | INTRADERMAL, SUBCUTANEOUS | 0.1 g in 1 mL | 12/9/2009 | |
| Antigen Laboratories, Inc. | 49288-0572 | SUBCUTANEOUS, INTRADERMAL | 0.05 g in 1 mL | 11/17/2009 |
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 |
|---|---|---|---|---|---|
| Hilde Hemmes' Herbals Elimo-Cough Teabags | 336232 | Medicine | A | 5/12/2020 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| RICOLA SWISS HERB COUGH DROPORANGE MINT | ricola ltd. | 01943766 | Lozenge - Oral | 0.5 MG | 12/31/1993 |
| CHEST AND COUGH HERB TEA NO 2 DR SCHIEFFER | dr nachf dr. nachf grunitz chemische erzeugnisse | 00218278 | Tea (Herbal) - Oral | 5 % | 12/31/1951 |
| HERBON COUGH DROPS GLACIAL MINT | herbon naturals inc. | 02231756 | Drops - Oral | 2 MG / DROP | 9/8/1997 |
| HOMEOPATHIC THROAT SPRAY | herbalife international of america, inc. | 02239375 | Spray - Oral | 1 X / X | 11/1/1999 |
| LIQUISAN SYR FOR COUGH NO2 | a g kunzle krauterpfarrer ag | 00125520 | Syrup - Oral | 2 % | 12/31/1951 |
| VITALP PLUS EUCALYPTUS | domaco dr med aufdermaur ag | 02237554 | Lozenge - Oral | 52.14 MG / LOZ | N/A |
| HERBAL DECONGESTANT EXPECTORANT - CAP | vita health products inc | 02225530 | Capsule - Oral | 400 MG / CAP | 9/8/1997 |
| THYMUS VULGARIS GOUTTE 4CH-30CH | dolisos laboratoires s.a. | 00690961 | Drops - Oral | 1 DH / DH | 12/31/1987 |
| CLEAR CAPSULES | awareness corporation | 02240022 | Capsule - Oral | 37.5 MG / CAP | 2/10/2001 |
| MOUNTAIN BREEZE SWISS HERBS COUGH DROPS | ricola ltd. | 02245759 | Lozenge - Oral | 15.75 MG | 4/13/2002 |
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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