0.9% sodium chloride

Generic: sodium chloride

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

Drug Facts

Product Profile

Brand Name 0.9% sodium chloride
Generic Name sodium chloride
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 9 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1577
Product ID 51662-1577_c755e41b-acbb-7234-e053-2995a90aff0f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207310
Listing Expiration 2026-12-31
Marketing Start 2021-07-17

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 516621577
Hyphenated Format 51662-1577

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 0.9% sodium chloride (source: ndc)
Generic Name sodium chloride (source: ndc)
Application Number ANDA207310 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 9 mg/mL
source: ndc
Packaging
  • 500 mL in 1 BAG (51662-1577-1)
source: ndc

Packages (1)

51662-1577-1 500 mL in 1 BAG (51662-1577-1)

Ingredients (1)

sodium chloride (9 mg/mL)

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": "c755e41b-acbb-7234-e053-2995a90aff0f", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807634"], "spl_set_id": ["c755e41b-acba-7234-e053-2995a90aff0f"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (51662-1577-1)", "package_ndc": "51662-1577-1", "marketing_start_date": "20210717"}], "brand_name": "0.9% SODIUM CHLORIDE", "product_id": "51662-1577_c755e41b-acbb-7234-e053-2995a90aff0f", "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": "51662-1577", "generic_name": "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": "9 mg/mL"}], "application_number": "ANDA207310", "marketing_category": "ANDA", "marketing_start_date": "20210717", "listing_expiration_date": "20261231"}