Potassium Citrate (Upsher-Smith Laboratories, LLC)
Welcome to the PulseAid listing for the Potassium Citrate drug offered from Upsher-Smith Laboratories, LLC. 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: | Upsher-Smith Laboratories, LLC |
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 |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2006-09-01 |
END MARKETING DATE: | 0000-00-00 |
Potassium Citrate HUMAN PRESCRIPTION DRUG Details:
Item Description | Potassium Citrate from Upsher-Smith Laboratories, LLC |
LABELER NAME: | Upsher-Smith Laboratories, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5(meq/1) |
START MARKETING DATE: | 2006-09-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0245-0070_65e63e06-e105-4134-b074-5040687bf359 |
PRODUCT NDC: | 0245-0070 |
APPLICATION NUMBER: | NDA019071 |
Other POTASSIUM CITRATE Pharmaceutical Manufacturers / Labelers: