ColPrep Kit (KVK-Tech, Inc.)
Welcome to the PulseAid listing for the ColPrep Kit drug offered from KVK-Tech, Inc.. This Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | KVK-Tech, Inc. |
| NON-PROPRIETARY NAME: | sodium sulfate, potassium sulfate, and magnesium sulfate for oral solution |
| SUBSTANCE NAME: | SODIUM SULFATE; POTASSIUM SULFATE; MAGNESIUM SULFATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] |
| ROUTE: | ORAL |
| DOSAGE FORM: | POWDER, FOR SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2016-12-27 |
| END MARKETING DATE: | 0000-00-00 |
ColPrep Kit HUMAN PRESCRIPTION DRUG Details:
| Item Description | ColPrep Kit from KVK-Tech, Inc. |
| LABELER NAME: | KVK-Tech, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 17.5; 3.13; 1.6(g/22.7g; g/22.7g; g/22.7g) |
| START MARKETING DATE: | 2016-12-27 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 10702-283_767105a0-65a5-444a-989f-f766b0851c2a |
| PRODUCT NDC: | 10702-283 |
| APPLICATION NUMBER: | NDA204553 |
Other SODIUM SULFATE; POTASSIUM SULFATE; MAGNESIUM SULFATE Pharmaceutical Manufacturers / Labelers:
