Potassium Citrate (American Health Packaging)
Welcome to the PulseAid listing for the Potassium Citrate drug offered from American Health Packaging. 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: | American Health Packaging |
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: | 2014-10-01 |
END MARKETING DATE: | 0000-00-00 |
Potassium Citrate HUMAN PRESCRIPTION DRUG Details:
Item Description | Potassium Citrate from American Health Packaging |
LABELER NAME: | American Health Packaging |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(meq/1) |
START MARKETING DATE: | 2014-10-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68084-850_ad39bed0-b723-4d0b-a238-46737420d6d1 |
PRODUCT NDC: | 68084-850 |
APPLICATION NUMBER: | ANDA203546 |
Other POTASSIUM CITRATE Pharmaceutical Manufacturers / Labelers: