sodium chloride

Generic: sodium chloride

Labeler: spectra medical deviecs, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler spectra medical deviecs, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

sodium chloride 9 mg/mL

Manufacturer
Spectra Medical Deviecs, LLC

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
1807637 1807646
UNII
451W47IQ8X

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 9 mg/mL
source: ndc
Packaging
  • 5 TRAY in 1 CARTON (65282-1510-1) / 5 AMPULE in 1 TRAY / 10 mL in 1 AMPULE
source: ndc

Packages (1)

Ingredients (1)

sodium chloride (9 mg/mL)

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"}