UROCIT-K (REMEDYREPACK INC.)
Welcome to the PulseAid listing for the UROCIT-K drug offered from REMEDYREPACK INC.. This Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA] 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: | REMEDYREPACK INC. |
| NON-PROPRIETARY NAME: | potassium citrate |
| SUBSTANCE NAME: | POTASSIUM CITRATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2016-12-28 |
| END MARKETING DATE: | 0000-00-00 |
UROCIT-K HUMAN PRESCRIPTION DRUG Details:
| Item Description | UROCIT-K from REMEDYREPACK INC. |
| LABELER NAME: | REMEDYREPACK INC. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(meq/1) |
| START MARKETING DATE: | 2016-12-28 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 70518-0086_5ccd86c2-a110-49a8-e053-2a91aa0a68fb |
| PRODUCT NDC: | 70518-0086 |
| APPLICATION NUMBER: | NDA019071 |
Other POTASSIUM CITRATE Pharmaceutical Manufacturers / Labelers:
