0409-1130 NDC - SODIUM CHLORIDE ()

Drug Information

  • Product NDC: 0409-1130
  • Proprietary Name: Sodium Chloride
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Hospira, Inc.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:5/26/2005
End Marketing Date:5/1/2011

Package Information

No. Package Code Package Description Billing Unit
10409-1130-0212 BOTTLE, GLASS in 1 CASE (0409-1130-02) / 250 mL in 1 BOTTLE, GLASSML

NDC Record

Field Name Field Value Definition
PRODUCT NDC0409-1130The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
PROPRIETARY NAMESodium ChlorideThis is the date that the labeler indicates was the start of its marketing of the drug product.
START MARKETING DATE5/26/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE5/1/2011Product 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.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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 NAMEHospira, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025

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