0.9% sodium chloride

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

sodium chloride 9 g/1000mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1609
Product ID 51662-1609_0ffa8cc4-f3fa-0814-e063-6294a90a9234
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207956
Listing Expiration 2026-12-31
Marketing Start 2022-07-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621609
Hyphenated Format 51662-1609

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 0.9% sodium chloride (source: ndc)
Application Number ANDA207956 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 9 g/1000mL
source: ndc
Packaging
  • 500 mL in 1 BAG (51662-1609-1)
source: ndc

Packages (1)

51662-1609-1 500 mL in 1 BAG (51662-1609-1)

Ingredients (1)

sodium chloride (9 g/1000mL)

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": "0ffa8cc4-f3fa-0814-e063-6294a90a9234", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807634"], "spl_set_id": ["e5247ed5-6170-c13f-e053-2a95a90a4101"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (51662-1609-1)", "package_ndc": "51662-1609-1", "marketing_start_date": "20220731"}], "brand_name": "0.9% SODIUM CHLORIDE", "product_id": "51662-1609_0ffa8cc4-f3fa-0814-e063-6294a90a9234", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1609", "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": "9 g/1000mL"}], "application_number": "ANDA207956", "marketing_category": "ANDA", "marketing_start_date": "20220731", "listing_expiration_date": "20261231"}