sodium chloride

Generic: sodium chloride

Labeler: henry schein, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler henry schein, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

sodium chloride 9 mg/mL

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9954
Product ID 0404-9954_82fec5d4-5c84-487c-b59a-ed8fab299d2b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018803
Listing Expiration 2026-12-31
Marketing Start 2022-01-12

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 04049954
Hyphenated Format 0404-9954

Supplemental Identifiers

RxCUI
1807631 1807638
UNII
451W47IQ8X

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 NDA018803 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 9 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9954-20) / 20 mL in 1 VIAL, SINGLE-DOSE
  • 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9954-50) / 50 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (2)

0404-9954-20 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9954-20) / 20 mL in 1 VIAL, SINGLE-DOSE 0404-9954-50 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9954-50) / 50 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

sodium chloride (9 mg/mL)

Linked Drug Pages (1)

Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "82fec5d4-5c84-487c-b59a-ed8fab299d2b", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807631", "1807638"], "spl_set_id": ["d8b8d796-bfba-42af-a859-99d776871558"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9954-20)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9954-20", "marketing_start_date": "20220112"}, {"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9954-50)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9954-50", "marketing_start_date": "20220112"}], "brand_name": "Sodium Chloride", "product_id": "0404-9954_82fec5d4-5c84-487c-b59a-ed8fab299d2b", "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": "0404-9954", "generic_name": "Sodium Chloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "NDA018803", "marketing_category": "NDA", "marketing_start_date": "20220112", "listing_expiration_date": "20261231"}