Package 14789-134-05

Brand: Sodium Chloride

Generic: Sodium Chloride
NDC Package

Package Facts

Identity

Package NDC 14789-134-05
Digits Only 1478913405
Product NDC 14789-134
Product ID 14789-134_236c8a25-1a66-38f6-e063-6394a90ac855
Description

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

Marketing

Marketing Status
Discontinued 2026-02-28
Brand Sodium Chloride
Generic Sodium Chloride
Sample Package No

Linked Drug Pages (1)

Sodium Chloride ndc-match (0.95)

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"}