ACD-A (Fenwal Inc)


Welcome to the PulseAid listing for the ACD-A drug offered from Fenwal 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: Fenwal Inc
NON-PROPRIETARY NAME: Anticoagulant Citrate Dextrose Solution Formula A
SUBSTANCE NAME: DEXTROSE MONOHYDRATE; SODIUM CITRATE; ANHYDROUS CITRIC ACID
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: 2007-03-01
END MARKETING DATE: 0000-00-00


ACD-A HUMAN PRESCRIPTION DRUG Details:

Item DescriptionACD-A from Fenwal Inc
LABELER NAME: Fenwal Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 24.5; 22; 7.3(g/1000mL; g/1000mL; g/1000mL)
START MARKETING DATE: 2007-03-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0942-0641_1f546c80-456a-4fd7-984a-902a0a4305f6
PRODUCT NDC: 0942-0641
APPLICATION NUMBER: BN160918

Other DEXTROSE MONOHYDRATE; SODIUM CITRATE; ANHYDROUS CITRIC ACID Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Fenwal IncACD-A
Fenwal Inc.ACD-A