Sodium Citrate (Haemonetics Manufacturing Inc)
Welcome to the PulseAid listing for the Sodium Citrate 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] 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: | Anticoagulant Sodium Citrate Solution |
SUBSTANCE NAME: | SODIUM 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: | INTRAVENOUS |
DOSAGE FORM: | SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1978-06-30 |
END MARKETING DATE: | 0000-00-00 |
Sodium Citrate HUMAN PRESCRIPTION DRUG Details:
Item Description | Sodium Citrate from Haemonetics Manufacturing Inc |
LABELER NAME: | Haemonetics Manufacturing Inc |
DEA SCHEDULE: | CII
|
ACTIVE STRENGTH: | 10(g/250mL) |
START MARKETING DATE: | 1978-06-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 53157-798_1a2ad203-63fe-42ac-88c6-23dd28385005 |
PRODUCT NDC: | 53157-798 |
APPLICATION NUMBER: | NDA760305 |
Other SODIUM CITRATE Pharmaceutical Manufacturers / Labelers: