sodium chloride
Generic: sodium chloride
Labeler: spectra medical deviecs, llcDrug Facts
Product Profile
Brand Name
sodium chloride
Generic Name
sodium chloride
Labeler
spectra medical deviecs, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium chloride 9 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
65282-1510
Product ID
65282-1510_447bf261-1a3a-2da1-e063-6394a90a7537
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206171
Listing Expiration
2026-12-31
Marketing Start
2017-07-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
652821510
Hyphenated Format
65282-1510
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA206171 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 9 mg/mL
Packaging
- 5 TRAY in 1 CARTON (65282-1510-1) / 5 AMPULE in 1 TRAY / 10 mL in 1 AMPULE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "447bf261-1a3a-2da1-e063-6394a90a7537", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807637", "1807646"], "spl_set_id": ["7e316d21-d6ad-4976-bd90-268fd7e51361"], "manufacturer_name": ["Spectra Medical Deviecs, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 TRAY in 1 CARTON (65282-1510-1) / 5 AMPULE in 1 TRAY / 10 mL in 1 AMPULE", "package_ndc": "65282-1510-1", "marketing_start_date": "20170721"}], "brand_name": "Sodium Chloride", "product_id": "65282-1510_447bf261-1a3a-2da1-e063-6394a90a7537", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "65282-1510", "generic_name": "Sodium Chloride", "labeler_name": "Spectra Medical Deviecs, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "ANDA206171", "marketing_category": "ANDA", "marketing_start_date": "20170721", "listing_expiration_date": "20261231"}