Overview
No overview information available.
Indication
Used to treat constipation or to clean the bowel before a colonoscopy .
Associated Conditions
- Constipation
- Hypophosphatemia
- Severe constipation
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 |
|---|---|---|---|---|---|
| ICU Medical Inc. | 0990-7372 | INTRAVENOUS | 25 mg in 100 mL | 3/8/2021 | |
| Terumo BCT, Ltd | 14537-833 | INTRAVENOUS | 0.28 g in 100 mL | 12/15/2021 | |
| Meda Pharmaceuticals | 0037-6321 | ORAL | 40.8 mg in 1 1 | 1/13/2015 | |
| Star Pharmaceuticals, LLC | 0076-0111 | ORAL | 40.8 mg in 1 1 | 1/24/2017 | |
| A.G. Marin Pharmaceutical | 12539-144 | ORAL | 40.8 mg in 1 1 | 10/7/2022 | |
| Martin & Pleasance Pty Ltd | 84999-029 | ORAL | 6 [hp_X] in 1 1 | 9/9/2025 | |
| Terumo Corporation | 53877-001 | INTRAVENOUS | 2.22 g in 1000 mL | 12/7/2018 | |
| Haemonetics Corporation | 53157-736 | INTRAVENOUS | 0.14 g in 63 mL | 7/19/2023 | |
| Terumo Corporation | 53877-001 | INTRAVENOUS | 2.22 g in 1000 mL | 12/7/2018 | |
| Terumo BCT, Ltd | 14537-828 | INTRAVENOUS | 0.28 g in 100 mL | 7/18/2018 |
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 |
|---|---|---|---|---|---|
| TAMIPOOL FOR INJECTION | SIN11849P | INJECTION, POWDER, FOR SOLUTION | 3.6 mg/vial | 3/15/2002 |
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 |
|---|---|---|---|---|---|
| No TGA approvals found for this drug. | |||||
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| VERMOPT | terra botanica products ltd. | 02233378 | Liquid - Oral | 12 X | 5/25/1998 |
| TIS-U-SOL SOLUTION | baxter corporation | 00800007 | Liquid - Irrigation | 8.75 MG / 100 ML | 12/31/1990 |
| HOMOEP TAB CAL MAG POT SOD PHOSPH POT CHLOR | new era lab c/o seven seas | 00147117 | Tablet - Oral | .014 MCG / TAB | 12/31/1966 |
| ZIEF HOMOEOPATHIC TAB | new era lab c/o seven seas | 00578630 | Tablet - Oral | 6 X / TAB | 12/31/1983 |
| MOI-STIR SPRAY | solvay pharma inc | 01944428 | Spray - Buccal | 0.28 MG / ML | 6/20/1997 |
| MOI-STIR ORAL SWABSTICKS | paladin pharma inc. | 02238697 | Liquid - Buccal | 0.28 MG / ML | 8/3/2001 |
| SODIUM PHOSPHATE LIQUID (S#132) | total health centre | 02197014 | Liquid - Sublingual | 1 X / ML | 6/1/1997 |
| S10 S10 NATRUM PHOSPHORICUM 3X TAB | dr reckeweg canada | 02075075 | Tablet - Oral | 3 X / TAB | 12/31/1994 |
| PHOSPHO-SODA BUFFERED SALINE LAXATIVE | c.b. fleet company inc. | 00771678 | Liquid - Oral | 900 MG / 5 ML | 12/31/1993 |
| NEUTRALITE LIQ | canadian custom packaging company | 00313467 | Liquid - Topical | 35.69575 Kg / 576 L | 12/31/1964 |
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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