CPDA-1 Blood Collection System (Haemonetics Manufacturing Inc)
Welcome to the PulseAid listing for the CPDA-1 Blood Collection System drug offered from Haemonetics Manufacturing 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] 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: | Haemonetics Manufacturing Inc |
| NON-PROPRIETARY NAME: | Blood Collection System |
| SUBSTANCE NAME: | DEXTROSE MONOHYDRATE; SODIUM CITRATE; CITRIC ACID MONOHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; ADENINE |
| 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] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1980-11-06 |
| END MARKETING DATE: | 0000-00-00 |
CPDA-1 Blood Collection System HUMAN PRESCRIPTION DRUG Details:
| Item Description | CPDA-1 Blood Collection System from Haemonetics Manufacturing Inc |
| LABELER NAME: | Haemonetics Manufacturing Inc |
| DEA SCHEDULE: | CII
|
| ACTIVE STRENGTH: | 2.23; 1.84; .229; .155; .019(g/70mL; g/70mL; g/70mL; g/70mL; g/70mL) |
| START MARKETING DATE: | 1980-11-06 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 53157-130_145f874d-bba2-42b7-a7f5-63c43bce506e |
| PRODUCT NDC: | 53157-130 |
| APPLICATION NUMBER: | NDA800077 |
Other DEXTROSE MONOHYDRATE; SODIUM CITRATE; CITRIC ACID MONOHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; ADENINE Pharmaceutical Manufacturers / Labelers:
