0338-6304 NDC - SODIUM CHLORIDE ()

Drug Information

Product NDC: 0338-6304
Proprietary Name: Sodium Chloride
Non Proprietary Name:
Active Ingredient(s):
Administration Route(s):
Dosage Form(s):

Labeler Information

Field Name	Field Value
Labeler Name:	Baxter Healthcare Corporation
Product Type:
FDA Application Number:	NDA016677
Marketing Category:	NDA
Start Marketing Date:	12/9/1970
End Marketing Date:	6/30/2017

Package Information

No.	Package Code	Package Description	Billing Unit
1	0338-6304-02	250 mL in 1 BAG (0338-6304-02)	ML
2	0338-6304-03	500 mL in 1 BAG (0338-6304-03)	ML
3	0338-6304-04	1000 mL in 1 BAG (0338-6304-04)	ML

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	0338-6304	Product 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.
PROPRIETARY NAME	Sodium Chloride	This 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.
START MARKETING DATE	12/9/1970	Name of Company corresponding to the labeler code segment of the Product NDC.
END MARKETING DATE	6/30/2017	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
MARKETING CATEGORY NAME	NDA	Product 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 NUMBER	NDA016677	This 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 NAME	Baxter Healthcare Corporation	Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record record in Text format: Export

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

Download this NDC record record in XML format: Export

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

Previous Code

Next Code