sodium chloride

Generic: sodium chloride

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 900 mg/100mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1522
Product ID 51662-1522_ac0fd44a-3f3a-8d7e-e053-2995a90afeec
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA016366
Listing Expiration 2026-12-31
Marketing Start 2020-08-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621522
Hyphenated Format 51662-1522

Supplemental Identifiers

RxCUI
1807634
UNII
451W47IQ8X

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 NDA016366 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 900 mg/100mL
source: ndc
Packaging
  • 500 mL in 1 BAG (51662-1522-1)
source: ndc

Packages (1)

51662-1522-1 500 mL in 1 BAG (51662-1522-1)

Ingredients (1)

sodium chloride (900 mg/100mL)

Linked Drug Pages (1)

SODIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ac0fd44a-3f3a-8d7e-e053-2995a90afeec", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807634"], "spl_set_id": ["ac0fd44a-3f39-8d7e-e053-2995a90afeec"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (51662-1522-1)", "package_ndc": "51662-1522-1", "marketing_start_date": "20200804"}], "brand_name": "SODIUM CHLORIDE", "product_id": "51662-1522_ac0fd44a-3f3a-8d7e-e053-2995a90afeec", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1522", "generic_name": "SODIUM CHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM CHLORIDE", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "900 mg/100mL"}], "application_number": "NDA016366", "marketing_category": "NDA", "marketing_start_date": "20200804", "listing_expiration_date": "20261231"}