TRICITRATES (Pharmaceutical Associates, Inc.)
Welcome to the PulseAid listing for the TRICITRATES drug offered from Pharmaceutical Associates, Inc.. This Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],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: | Pharmaceutical Associates, Inc. |
| NON-PROPRIETARY NAME: | POTASSIUM CITRATE, SODIUM CITRATE, and CITRIC ACID MONOHYDRATE |
| SUBSTANCE NAME: | POTASSIUM CITRATE; SODIUM CITRATE; CITRIC ACID MONOHYDRATE |
| 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],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | SOLUTION |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2005-05-25 |
| END MARKETING DATE: | 0000-00-00 |
TRICITRATES HUMAN PRESCRIPTION DRUG Details:
| Item Description | TRICITRATES from Pharmaceutical Associates, Inc. |
| LABELER NAME: | Pharmaceutical Associates, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 550; 500; 334(mg/5mL; mg/5mL; mg/5mL) |
| START MARKETING DATE: | 2005-05-25 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0121-0677_57e16fd9-afb8-498f-9c46-ebd46cfaedc4 |
| PRODUCT NDC: | 0121-0677 |
| APPLICATION NUMBER: | |
Other POTASSIUM CITRATE; SODIUM CITRATE; CITRIC ACID MONOHYDRATE Pharmaceutical Manufacturers / Labelers:
