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 |
---|---|---|---|---|---|
Cantrell Drug Company | 52533-174 | EPIDURAL | N/A | 1/13/2015 | |
Cantrell Drug Company | 52533-166 | INTRAVENOUS | N/A | 3/6/2015 | |
Novo Nordisk | 0169-3205 | SUBCUTANEOUS | N/A | 6/21/2023 | |
Mylan Institutional LLC | 67457-585 | SUBCUTANEOUS | N/A | 8/15/2020 | |
Cantrell Drug Company | 52533-211 | INTRAVENOUS | N/A | 12/24/2014 | |
Cantrell Drug Company | 52533-025 | INTRAVENOUS | N/A | 8/13/2014 | |
Mylan Institutional LLC | 67457-593 | SUBCUTANEOUS | N/A | 6/8/2020 | |
Cantrell Drug Company | 52533-001 | INTRAVENOUS | N/A | 1/14/2016 | |
Bryant Ranch Prepack | 63629-8744 | INTRAMUSCULAR | N/A | 8/24/2021 | |
Mylan Institutional LLC | 67457-594 | SUBCUTANEOUS | N/A | 6/8/2020 |
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 |
---|---|---|---|---|---|
GALLIAPHARM RADIONUCLIDE GENERATOR 1.11 - 1.85 GBQ | N/A | N/A | N/A | 10/11/2024 |
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 |
---|---|---|---|---|---|
FERRUM / ACIDUM CHOLALICUM | weleda ag heilmittelbetriebe | 02232595 | Powder
,
Liquid - Oral | 4 D | 3/4/1998 |
MURIATICUM ACIDUM DROPS (C6-C1000) | thompson's homeopathic supplies ltd. | 01954725 | Drops - Oral | 6 C / C | 12/31/1992 |
MURIATICUM ACIDUM | dolisos canada inc. | 02234616 | Granules
,
Globules
,
Liquid - Oral | 6 X | 1/5/1998 |
MURIATICUM ACIDUM | seroyal international inc. | 02233786 | Liquid
,
Globules
,
Tablet
,
Granules
,
Drops
,
Pellet - Oral | 6 X | 4/6/1998 |
MURIATICUM ACIDUM GRANULE 1CH - 30CH | dolisos laboratoires s.a. | 00698253 | Tablet - Oral | 1 CH / CH | 12/31/1987 |
HOMEODEX 09 | distributions biodentcom inc. | 02232215 | Granules - Oral | 18 D | 6/3/1998 |
MURIATICUM ACID GRANULES 1DH | homeocan inc. | 00866830 | Tablet - Oral | 1 DH / DH | 12/31/1989 |
L OPT | terra botanica products ltd. | 02233342 | Liquid - Oral | 12 X | 6/3/1998 |
EV TOX | bio active canada ltd. | 02234235 | Liquid - Oral | 12 X | 5/26/1998 |
MURIATICUM ACID GLOBULES 2CH-30CH | boiron laboratoires | 00670456 | Tablet - Oral | 2 CH / CH | 12/31/1986 |
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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