3% sodium chloride

Generic: 3% sodium chloride

Labeler: becton dickinson and company
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name 3% sodium chloride
Generic Name 3% sodium chloride
Labeler becton dickinson and company
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 3 g/100mL

Manufacturer
Becton Dickinson and Company

Identifiers & Regulatory

Product NDC 17271-703
Product ID 17271-703_ab3d79da-7b4a-4224-b0e4-46bd00bf6444
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209476
Listing Expiration 2026-12-31
Marketing Start 2020-02-28

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 17271703
Hyphenated Format 17271-703

Supplemental Identifiers

RxCUI
730781
UNII
451W47IQ8X

Packaging Origin

Original Packager
true

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 3% sodium chloride (source: ndc)
Generic Name 3% sodium chloride (source: ndc)
Application Number ANDA209476 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 3 g/100mL
source: ndc
Packaging
  • 20 BAG in 1 CASE (17271-703-06) / 500 mL in 1 BAG
source: ndc

Packages (1)

17271-703-06 20 BAG in 1 CASE (17271-703-06) / 500 mL in 1 BAG

Ingredients (1)

sodium chloride (3 g/100mL)

Linked Drug Pages (1)

3% Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ab3d79da-7b4a-4224-b0e4-46bd00bf6444", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["730781"], "spl_set_id": ["a8058593-48af-457a-b0f0-166935c7d10c"], "manufacturer_name": ["Becton Dickinson and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BAG in 1 CASE (17271-703-06)  / 500 mL in 1 BAG", "package_ndc": "17271-703-06", "marketing_start_date": "20200228"}], "brand_name": "3% Sodium Chloride", "product_id": "17271-703_ab3d79da-7b4a-4224-b0e4-46bd00bf6444", "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": "17271-703", "generic_name": "3% Sodium Chloride", "labeler_name": "Becton Dickinson and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "3% Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "3 g/100mL"}], "application_number": "ANDA209476", "marketing_category": "ANDA", "marketing_start_date": "20200228", "listing_expiration_date": "20261231"}