sodium chloride

Generic: sodium chloride

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

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

sodium chloride 9 mg/mL

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-083
Product ID 76420-083_b8e8faa1-b133-450e-e053-2995a90aeace
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018803
Listing Expiration 2026-12-31
Marketing Start 2005-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420083
Hyphenated Format 76420-083

Supplemental Identifiers

RxCUI
1807637
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
  • 10 mL in 1 VIAL, SINGLE-DOSE (76420-083-10)
source: ndc

Packages (1)

76420-083-10 10 mL in 1 VIAL, SINGLE-DOSE (76420-083-10)

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": "b8e8faa1-b133-450e-e053-2995a90aeace", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807637"], "spl_set_id": ["a411c118-ef0e-4c42-9924-4a06ec690e94"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (76420-083-10)", "package_ndc": "76420-083-10", "marketing_start_date": "20200409"}], "brand_name": "Sodium Chloride", "product_id": "76420-083_b8e8faa1-b133-450e-e053-2995a90aeace", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "76420-083", "generic_name": "Sodium Chloride", "labeler_name": "Asclemed USA, 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": "20050228", "listing_expiration_date": "20261231"}