sodium chloride
Generic: sodium chloride
Labeler: medical purchasing solutions, llcDrug Facts
Product Profile
Brand Name
sodium chloride
Generic Name
sodium chloride
Labeler
medical purchasing solutions, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium chloride 9 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71872-7248
Product ID
71872-7248_c3f8e83c-4fba-91da-e053-2a95a90abd63
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
718727248
Hyphenated Format
71872-7248
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 9 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7248-1) / 20 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "c3f8e83c-4fba-91da-e053-2a95a90abd63", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807638"], "spl_set_id": ["c3f8e83c-4fb9-91da-e053-2a95a90abd63"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (71872-7248-1) / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71872-7248-1", "marketing_start_date": "20210331"}], "brand_name": "Sodium Chloride", "product_id": "71872-7248_c3f8e83c-4fba-91da-e053-2a95a90abd63", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "71872-7248", "generic_name": "Sodium Chloride", "labeler_name": "Medical Purchasing Solutions, LLC", "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"}