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
INJECTION, SOLUTION
Routes
Active Ingredients
sodium chloride 4.5 g/1000mL
Manufacturer
Identifiers & Regulatory
Product NDC
0338-0043
Product ID
0338-0043_8edef896-cfdd-43fe-a358-f4f82642c4c5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018016
Listing Expiration
2027-12-31
Marketing Start
1979-02-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03380043
Hyphenated Format
0338-0043
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
NDA018016 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4.5 g/1000mL
Packaging
- 500 mL in 1 BAG (0338-0043-03)
- 1000 mL in 1 BAG (0338-0043-04)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "8edef896-cfdd-43fe-a358-f4f82642c4c5", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807551", "1807552", "1807627", "1807630", "1807631", "1807632", "1807633", "1807634", "1807639"], "spl_set_id": ["f55bd888-5e01-474d-871b-24654c070178"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (0338-0043-03)", "package_ndc": "0338-0043-03", "marketing_start_date": "19790202"}, {"sample": false, "description": "1000 mL in 1 BAG (0338-0043-04)", "package_ndc": "0338-0043-04", "marketing_start_date": "19790202"}], "brand_name": "Sodium Chloride", "product_id": "0338-0043_8edef896-cfdd-43fe-a358-f4f82642c4c5", "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": "0338-0043", "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": "4.5 g/1000mL"}], "application_number": "NDA018016", "marketing_category": "NDA", "marketing_start_date": "19790202", "listing_expiration_date": "20271231"}