0.9% sodium chloride

Generic: 0.9% sodium chloride

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

Drug Facts

Product Profile

Brand Name 0.9% sodium chloride
Generic Name 0.9% 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 51662-1517
Product ID 51662-1517_a2b8220f-e33b-51c3-e053-2995a90a0734
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA016366
Listing Expiration 2026-12-31
Marketing Start 2020-04-07

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621517
Hyphenated Format 51662-1517

Supplemental Identifiers

RxCUI
1807633
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 0.9% sodium chloride (source: ndc)
Generic Name 0.9% sodium chloride (source: ndc)
Application Number NDA016366 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 900 mg/100mL
source: ndc
Packaging
  • 1 BAG in 1 POUCH (51662-1517-1) / 250 mL in 1 BAG
source: ndc

Packages (1)

51662-1517-1 1 BAG in 1 POUCH (51662-1517-1) / 250 mL in 1 BAG

Ingredients (1)

sodium chloride (900 mg/100mL)

Linked Drug Pages (1)

0.9% SODIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "a2b8220f-e33b-51c3-e053-2995a90a0734", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807633"], "spl_set_id": ["a2b8220f-e33a-51c3-e053-2995a90a0734"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BAG in 1 POUCH (51662-1517-1)  / 250 mL in 1 BAG", "package_ndc": "51662-1517-1", "marketing_start_date": "20200407"}], "brand_name": "0.9% SODIUM CHLORIDE", "product_id": "51662-1517_a2b8220f-e33b-51c3-e053-2995a90a0734", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "51662-1517", "generic_name": "0.9% SODIUM CHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "0.9% SODIUM CHLORIDE", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "900 mg/100mL"}], "application_number": "NDA016366", "marketing_category": "NDA", "marketing_start_date": "20200407", "listing_expiration_date": "20261231"}