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: Antiocoagulant 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: 2012-10-24
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: 2.45; 2.2; 730(g/100mL; g/100mL; mg/100mL)
START MARKETING DATE: 2012-10-24
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0942-9005_bf4444ef-bff1-46c8-b11d-99091f14262d
PRODUCT NDC: 0942-9005
APPLICATION NUMBER: BN160918

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

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