0338-9556 NDC - HEPARIN SODIUM AND SODIUM CHLORIDE (HEPARIN SODIUM)

Drug Information

Product NDC: 0338-9556

Proprietary Name: Heparin Sodium and Sodium Chloride

Non Proprietary Name: heparin sodium

Active Ingredient(s):
  • 1000 [iU]/500mL HEPARIN SODIUM


Administration Route(s): INTRAVENOUS

Dosage Form(s): INJECTION, SOLUTION

Pharmacy Class(es):
  • Anti-coagulant [EPC];
  • Heparin [CS];
  • Unfractionated Heparin [EPC]

Labeler Information

Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Start Marketing Date:10/25/2017

Package Information

No. Package Code Package Description Billing Unit
10338-9556-2020 BAG in 1 CARTON (0338-9556-20) > 500 mL in 1 BAGML

NDC Record

Field Name Field Value Definition
PRODUCT NDC0338-9556The 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 NAMEHeparin Sodium and Sodium ChlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEheparin sodiumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEINJECTION, SOLUTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEINTRAVENOUSThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE10/25/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG FOR USE IN DRUG SHORTAGEProduct 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.
LABELER NAMEBaxter Healthcare CorporationName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEHEPARIN SODIUMThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH1000 
ACTIVE INGRED UNIT[iU]/500mL 
PHARM CLASSESAnti-coagulant [EPC],Heparin [CS],Unfractionated Heparin [EPC] 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 5/17/2019