sodium chloride
Generic: sodium chloride
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
sodium chloride
Generic Name
sodium chloride
Labeler
baxter healthcare corporation
Dosage Form
IRRIGANT
Routes
Active Ingredients
sodium chloride 900 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0338-0047
Product ID
0338-0047_e4fe8929-43e5-4e60-ba1f-34b84756974f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017867
Listing Expiration
2026-12-31
Marketing Start
1980-05-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03380047
Hyphenated Format
0338-0047
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 900 mg/100mL
Packaging
- 4 BAG in 1 CARTON (0338-0047-27) / 3000 mL in 1 BAG
- 2 BAG in 1 CARTON (0338-0047-29) / 5000 mL in 1 BAG
Packages (2)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["IRRIGATION"], "spl_id": "e4fe8929-43e5-4e60-ba1f-34b84756974f", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["486515"], "spl_set_id": ["05dee566-7b82-4216-8a6b-765d2b4d9dc7"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BAG in 1 CARTON (0338-0047-27) / 3000 mL in 1 BAG", "package_ndc": "0338-0047-27", "marketing_start_date": "19800530"}, {"sample": false, "description": "2 BAG in 1 CARTON (0338-0047-29) / 5000 mL in 1 BAG", "package_ndc": "0338-0047-29", "marketing_start_date": "19800530"}], "brand_name": "Sodium Chloride", "product_id": "0338-0047_e4fe8929-43e5-4e60-ba1f-34b84756974f", "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": "0338-0047", "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": "20261231"}