sodium chloride

Generic: sodium chloride

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler baxter healthcare corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 9 g/1000mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-9657
Product ID 0338-9657_ba9e58a5-60c5-4aab-9cef-36320d052091
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA016677
Listing Expiration 2027-12-31
Marketing Start 1970-12-09

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03389657
Hyphenated Format 0338-9657

Supplemental Identifiers

RxCUI
1807631 1807632 1807633 1807634 1807639
UNII
451W47IQ8X

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sodium chloride (source: ndc)
Generic Name sodium chloride (source: ndc)
Application Number NDA016677 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 9 g/1000mL
source: ndc
Packaging
  • 50 mL in 1 BAG (0338-9657-75)
source: ndc

Packages (1)

0338-9657-75 50 mL in 1 BAG (0338-9657-75)

Ingredients (1)

sodium chloride (9 g/1000mL)

Linked Drug Pages (1)

SODIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ba9e58a5-60c5-4aab-9cef-36320d052091", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807631", "1807632", "1807633", "1807634", "1807639"], "spl_set_id": ["958d35f0-6834-43be-a700-fa58f38b4c19"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BAG (0338-9657-75)", "package_ndc": "0338-9657-75", "marketing_start_date": "20240809"}], "brand_name": "SODIUM CHLORIDE", "product_id": "0338-9657_ba9e58a5-60c5-4aab-9cef-36320d052091", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0338-9657", "generic_name": "sodium chloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM CHLORIDE", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 g/1000mL"}], "application_number": "NDA016677", "marketing_category": "NDA", "marketing_start_date": "19701209", "listing_expiration_date": "20271231"}