dextrose and sodium chloride

Generic: dextrose monohydrate and sodium chloride

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

Drug Facts

Product Profile

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

dextrose monohydrate 5 g/100mL, sodium chloride .9 g/100mL

Manufacturer
BECTON DICKINSON AND COMPANY

Identifiers & Regulatory

Product NDC 17271-735
Product ID 17271-735_69075560-be94-4804-ab7b-d8ebce41739a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211211
Listing Expiration 2026-12-31
Marketing Start 2020-10-26

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 17271735
Hyphenated Format 17271-735

Supplemental Identifiers

RxCUI
1795344 1795346
UNII
LX22YL083G 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 dextrose and sodium chloride (source: ndc)
Generic Name dextrose monohydrate and sodium chloride (source: ndc)
Application Number ANDA211211 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • .9 g/100mL
source: ndc
Packaging
  • 20 BAG in 1 CASE (17271-735-06) / 500 mL in 1 BAG
  • 10 BAG in 1 CASE (17271-735-07) / 1000 mL in 1 BAG
source: ndc

Packages (2)

17271-735-06 20 BAG in 1 CASE (17271-735-06) / 500 mL in 1 BAG 17271-735-07 10 BAG in 1 CASE (17271-735-07) / 1000 mL in 1 BAG

Ingredients (2)

dextrose monohydrate (5 g/100mL) sodium chloride (.9 g/100mL)

Linked Drug Pages (1)

Dextrose and Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "69075560-be94-4804-ab7b-d8ebce41739a", "openfda": {"unii": ["LX22YL083G", "451W47IQ8X"], "rxcui": ["1795344", "1795346"], "spl_set_id": ["c1d0f42e-3494-4217-8f86-e9f34d930e82"], "manufacturer_name": ["BECTON DICKINSON AND COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BAG in 1 CASE (17271-735-06)  / 500 mL in 1 BAG", "package_ndc": "17271-735-06", "marketing_start_date": "20250515"}, {"sample": false, "description": "10 BAG in 1 CASE (17271-735-07)  / 1000 mL in 1 BAG", "package_ndc": "17271-735-07", "marketing_start_date": "20250515"}], "brand_name": "Dextrose and Sodium Chloride", "product_id": "17271-735_69075560-be94-4804-ab7b-d8ebce41739a", "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": "17271-735", "generic_name": "DEXTROSE MONOHYDRATE and SODIUM CHLORIDE", "labeler_name": "BECTON DICKINSON AND COMPANY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": ".9 g/100mL"}], "application_number": "ANDA211211", "marketing_category": "ANDA", "marketing_start_date": "20201026", "listing_expiration_date": "20261231"}