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
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

sodium chloride 9 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1464
Product ID 51662-1464_2b39dbc0-2d0b-0a7f-e063-6394a90add31
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018803
Listing Expiration 2026-12-31
Marketing Start 2019-12-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621464
Hyphenated Format 51662-1464

Supplemental Identifiers

RxCUI
1807638
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 NDA018803 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 9 mg/mL
source: ndc
Packaging
  • 20 mL in 1 VIAL, SINGLE-DOSE (51662-1464-1)
source: ndc

Packages (1)

51662-1464-1 20 mL in 1 VIAL, SINGLE-DOSE (51662-1464-1)

Ingredients (1)

sodium chloride (9 mg/mL)

Linked Drug Pages (1)

SODIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2b39dbc0-2d0b-0a7f-e063-6394a90add31", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807638"], "spl_set_id": ["998a2a47-5c79-2efd-e053-2995a90a8fac"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, SINGLE-DOSE (51662-1464-1)", "package_ndc": "51662-1464-1", "marketing_start_date": "20191212"}], "brand_name": "SODIUM CHLORIDE", "product_id": "51662-1464_2b39dbc0-2d0b-0a7f-e063-6394a90add31", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1464", "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": "9 mg/mL"}], "application_number": "NDA018803", "marketing_category": "NDA", "marketing_start_date": "20191212", "listing_expiration_date": "20261231"}