0942-6453 NDC - ADSOL RED CELL PRESERVATION SOLUTION SYSTEM IN PLASTIC CONTAINER (PL 146 PLASTIC) (ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE (CPD) SOLUTION AND ADSOL PRESERVATION SOLUTION)

Drug Information

Product NDC: 0942-6453

Proprietary Name: ADSOL Red Cell Preservation Solution System in Plastic Container (PL 146 Plastic)

Non Proprietary Name: Anticoagulant Citrate Phosphate Dextrose (CPD) Solution and ADSOL Preservation Solution

Active Ingredient(s):


Administration Route(s):

Dosage Form(s): KIT

Labeler Information

Labeler Name: Fenwal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BN811104
Marketing Category: NDA
Start Marketing Date:3/1/2007

Package Information

No. Package Code Package Description Billing Unit
10942-6453-031 KIT in 1 KIT (0942-6453-03) * 70 mL in 1 BAG * 110 mL in 1 BAG

NDC Record

Field Name Field Value Definition
PRODUCT NDC0942-6453The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEADSOL Red Cell Preservation Solution System in Plastic Container (PL 146 Plastic)The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAnticoagulant Citrate Phosphate Dextrose (CPD) Solution and ADSOL Preservation SolutionThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEKITThe translation of the dosage form Code submitted by the firm.
START MARKETING DATE3/1/2007This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMENDAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERBN811104This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEFenwal, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023