Sodium Chloride

Generic: Sodium Chloride

Labeler: Nexus Pharmaceuticals LLC
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Sodium Chloride
Generic Name Sodium Chloride
Labeler Nexus Pharmaceuticals LLC
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

SODIUM CHLORIDE 9 mg/mL

Identifiers & Regulatory

Product NDC 14789-134
Product ID 14789-134_236c8a25-1a66-38f6-e063-6394a90ac855
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217535
Marketing Start 2023-10-31
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 14789134
Hyphenated Format 14789-134

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 ANDA217535 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 9 mg/mL
source: ndc
Packaging
  • 25 VIAL, GLASS in 1 CARTON (14789-134-05) / 20 mL in 1 VIAL, GLASS (14789-134-07)
source: ndc

Packages (1)

14789-134-05 25 VIAL, GLASS in 1 CARTON (14789-134-05) / 20 mL in 1 VIAL, GLASS (14789-134-07)

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": "236c8a25-1a66-38f6-e063-6394a90ac855", "openfda": {"upc": ["0314789133058"], "unii": ["451W47IQ8X"], "rxcui": ["1807637", "1807638"], "spl_set_id": ["56455921-0c66-4d43-b993-3757b6983041"], "manufacturer_name": ["Nexus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, GLASS in 1 CARTON (14789-134-05)  / 20 mL in 1 VIAL, GLASS (14789-134-07)", "package_ndc": "14789-134-05", "marketing_end_date": "20260228", "marketing_start_date": "20231031"}], "brand_name": "Sodium Chloride", "product_id": "14789-134_236c8a25-1a66-38f6-e063-6394a90ac855", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "14789-134", "generic_name": "Sodium Chloride", "labeler_name": "Nexus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "ANDA217535", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20231031"}