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 SOLUTION
Routes
EXTRACORPOREAL
Active Ingredients

sodium chloride 900 mg/100mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-0050
Product ID 0338-0050_c0b84329-73d7-4f83-a6df-34b1e91b2dbf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA017867
Listing Expiration 2027-12-31
Marketing Start 1980-05-30

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 03380050
Hyphenated Format 0338-0050

Supplemental Identifiers

RxCUI
486515
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 NDA017867 (source: ndc)
Routes
EXTRACORPOREAL
source: ndc

Resolved Composition

Strengths
  • 900 mg/100mL
source: ndc
Packaging
  • 4 BAG in 1 CARTON (0338-0050-47) / 3000 mL in 1 BAG
source: ndc

Packages (1)

0338-0050-47 4 BAG in 1 CARTON (0338-0050-47) / 3000 mL in 1 BAG

Ingredients (1)

sodium chloride (900 mg/100mL)

Linked Drug Pages (1)

Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["EXTRACORPOREAL"], "spl_id": "c0b84329-73d7-4f83-a6df-34b1e91b2dbf", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["486515"], "spl_set_id": ["2a96096d-43cc-49b7-af53-b53c17f41001"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BAG in 1 CARTON (0338-0050-47)  / 3000 mL in 1 BAG", "package_ndc": "0338-0050-47", "marketing_start_date": "19800530"}], "brand_name": "Sodium Chloride", "product_id": "0338-0050_c0b84329-73d7-4f83-a6df-34b1e91b2dbf", "dosage_form": "SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0338-0050", "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": "900 mg/100mL"}], "application_number": "NDA017867", "marketing_category": "NDA", "marketing_start_date": "19800530", "listing_expiration_date": "20271231"}