63323-623 NDC - SODIUM CHLORIDE ()

Drug Information

  • Product NDC: 63323-623
  • Proprietary Name: Sodium Chloride
  • Non Proprietary Name:
  • Active Ingredient(s): 9 mg/mL SODIUM CHLORIDE
  • Administration Route(s):
  • Dosage Form(s):
  • Pharmacy Class(es): Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Fresenius Kabi USA, LLC
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Start Marketing Date:2/18/2014
End Marketing Date:11/14/2016

Package Information

No. Package Code Package Description Billing Unit
163323-623-0050 BAG in 1 BOX (63323-623-00) / 100 mL in 1 BAGML
263323-623-0950 BAG in 1 BOX (63323-623-09) / 100 mL in 1 BAGML
363323-623-1010 BAG in 1 BOX (63323-623-10) / 1000 mL in 1 BAGML
463323-623-5060 BAG in 1 BOX (63323-623-50) / 50 mL in 1 BAGML
563323-623-5120 BAG in 1 BOX (63323-623-51) / 500 mL in 1 BAGML
663323-623-5350 mL in 1 BAG (63323-623-53)ML
763323-623-5760 BAG in 1 BOX (63323-623-57) / 50 mL in 1 BAGML
863323-623-5920 BAG in 1 BOX (63323-623-59) / 500 mL in 1 BAGML
963323-623-61100 mL in 1 BAG (63323-623-61)ML
1063323-623-74250 mL in 1 BAG (63323-623-74)ML
1163323-623-75500 mL in 1 BAG (63323-623-75)ML
1263323-623-761000 mL in 1 BAG (63323-623-76)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC63323-623The 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.
PROPRIETARY NAMESodium ChlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/18/2014This 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 NAMEFresenius Kabi USA, LLCName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC63323-623The 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.
PROPRIETARY NAMESodium chlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/19/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct 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 NAMEFresenius Kabi USA, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/25/2025

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