sodium chloride

Generic: sodium chloride

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

Drug Facts

Product Profile

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

sodium chloride 9 mg/mL

Manufacturer
Becton Dickinson and Company

Identifiers & Regulatory

Product NDC 17271-701
Product ID 17271-701_31344de2-e115-440a-a913-ff63da5f17d8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207310
Listing Expiration 2026-12-31
Marketing Start 2017-09-19

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 17271701
Hyphenated Format 17271-701

Supplemental Identifiers

RxCUI
1807631 1807632 1807633 1807634 1807639
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 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
  • 50 mL in 1 BAG (17271-701-02)
  • 100 mL in 1 BAG (17271-701-03)
  • 250 mL in 1 BAG (17271-701-05)
  • 500 mL in 1 BAG (17271-701-06)
  • 1000 mL in 1 BAG (17271-701-07)
source: ndc

Packages (5)

17271-701-02 50 mL in 1 BAG (17271-701-02) 17271-701-03 100 mL in 1 BAG (17271-701-03) 17271-701-05 250 mL in 1 BAG (17271-701-05) 17271-701-06 500 mL in 1 BAG (17271-701-06) 17271-701-07 1000 mL in 1 BAG (17271-701-07)

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": ["INTRAVENOUS"], "spl_id": "31344de2-e115-440a-a913-ff63da5f17d8", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807631", "1807632", "1807633", "1807634", "1807639"], "spl_set_id": ["ebc8b008-a8b3-4c41-89e4-b413f7aab89f"], "manufacturer_name": ["Becton Dickinson and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BAG (17271-701-02)", "package_ndc": "17271-701-02", "marketing_start_date": "20170919"}, {"sample": false, "description": "100 mL in 1 BAG (17271-701-03)", "package_ndc": "17271-701-03", "marketing_start_date": "20170919"}, {"sample": false, "description": "250 mL in 1 BAG (17271-701-05)", "package_ndc": "17271-701-05", "marketing_start_date": "20170919"}, {"sample": false, "description": "500 mL in 1 BAG (17271-701-06)", "package_ndc": "17271-701-06", "marketing_start_date": "20170919"}, {"sample": false, "description": "1000 mL in 1 BAG (17271-701-07)", "package_ndc": "17271-701-07", "marketing_start_date": "20170919"}], "brand_name": "Sodium chloride", "product_id": "17271-701_31344de2-e115-440a-a913-ff63da5f17d8", "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": "17271-701", "generic_name": "SODIUM CHLORIDE", "labeler_name": "Becton Dickinson and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "ANDA207310", "marketing_category": "ANDA", "marketing_start_date": "20170919", "listing_expiration_date": "20261231"}