Potassium Citrate (Zydus Pharmaceuticals (USA) Inc.)
Welcome to the PulseAid listing for the Potassium Citrate drug offered from Zydus Pharmaceuticals (USA) 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: | Zydus Pharmaceuticals (USA) 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: | ANDA |
| START MARKETING DATE: | 2014-08-12 |
| END MARKETING DATE: | 0000-00-00 |
Potassium Citrate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Potassium Citrate from Zydus Pharmaceuticals (USA) Inc. |
| LABELER NAME: | Zydus Pharmaceuticals (USA) Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5(meq/1) |
| START MARKETING DATE: | 2014-08-12 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68382-536_df4421ad-772d-46cf-9fe9-c1b58060706a |
| PRODUCT NDC: | 68382-536 |
| APPLICATION NUMBER: | ANDA203546 |
Other POTASSIUM CITRATE Pharmaceutical Manufacturers / Labelers:
