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 IRRIGANT
Routes
IRRIGATION
Active Ingredients

sodium chloride 900 mg/100mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-0048
Product ID 0338-0048_1fe43459-21c4-4243-81bf-9674c1428f1e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA017427
Listing Expiration 2027-12-31
Marketing Start 1974-12-31

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 03380048
Hyphenated Format 0338-0048

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 NDA017427 (source: ndc)
Routes
IRRIGATION
source: ndc

Resolved Composition

Strengths
  • 900 mg/100mL
source: ndc
Packaging
  • 24 BOTTLE, PLASTIC in 1 CARTON (0338-0048-02) / 250 mL in 1 BOTTLE, PLASTIC
  • 18 BOTTLE, PLASTIC in 1 CARTON (0338-0048-03) / 500 mL in 1 BOTTLE, PLASTIC
  • 12 BOTTLE, PLASTIC in 1 CARTON (0338-0048-04) / 1000 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (3)

Ingredients (1)

sodium chloride (900 mg/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["IRRIGATION"], "spl_id": "1fe43459-21c4-4243-81bf-9674c1428f1e", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["486515"], "spl_set_id": ["b3b4b176-41f0-4ca8-90d4-3fba5707564a"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BOTTLE, PLASTIC in 1 CARTON (0338-0048-02)  / 250 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0338-0048-02", "marketing_start_date": "19741231"}, {"sample": false, "description": "18 BOTTLE, PLASTIC in 1 CARTON (0338-0048-03)  / 500 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0338-0048-03", "marketing_start_date": "19741231"}, {"sample": false, "description": "12 BOTTLE, PLASTIC in 1 CARTON (0338-0048-04)  / 1000 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0338-0048-04", "marketing_start_date": "19741231"}], "brand_name": "SODIUM CHLORIDE", "product_id": "0338-0048_1fe43459-21c4-4243-81bf-9674c1428f1e", "dosage_form": "IRRIGANT", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0338-0048", "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": "NDA017427", "marketing_category": "NDA", "marketing_start_date": "19741231", "listing_expiration_date": "20271231"}