dextrose and sodium chloride

Generic: dextrose and sodium chloride

Labeler: baxter healthcare company
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name dextrose and sodium chloride
Generic Name dextrose and sodium chloride
Labeler baxter healthcare company
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 5 g/100mL, sodium chloride 900 mg/100mL

Manufacturer
Baxter Healthcare Company

Identifiers & Regulatory

Product NDC 0338-0089
Product ID 0338-0089_b4404498-6ab7-4c25-a5a2-5377a6dfecca
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA016678
Listing Expiration 2026-12-31
Marketing Start 1970-12-09

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 03380089
Hyphenated Format 0338-0089

Supplemental Identifiers

RxCUI
1794881 1794886 1794887 1795250 1795252 1795344 1795346 1795470
UNII
451W47IQ8X LX22YL083G

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 and sodium chloride (source: ndc)
Application Number NDA016678 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • 900 mg/100mL
source: ndc
Packaging
  • 24 BAG in 1 CARTON (0338-0089-03) / 500 mL in 1 BAG
  • 14 BAG in 1 CARTON (0338-0089-04) / 1000 mL in 1 BAG
source: ndc

Packages (2)

0338-0089-03 24 BAG in 1 CARTON (0338-0089-03) / 500 mL in 1 BAG 0338-0089-04 14 BAG in 1 CARTON (0338-0089-04) / 1000 mL in 1 BAG

Ingredients (2)

dextrose monohydrate (5 g/100mL) sodium chloride (900 mg/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": "b4404498-6ab7-4c25-a5a2-5377a6dfecca", "openfda": {"unii": ["451W47IQ8X", "LX22YL083G"], "rxcui": ["1794881", "1794886", "1794887", "1795250", "1795252", "1795344", "1795346", "1795470"], "spl_set_id": ["dcbf1907-1841-4afc-ab5d-a9893a2d7256"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CARTON (0338-0089-03)  / 500 mL in 1 BAG", "package_ndc": "0338-0089-03", "marketing_start_date": "19701209"}, {"sample": false, "description": "14 BAG in 1 CARTON (0338-0089-04)  / 1000 mL in 1 BAG", "package_ndc": "0338-0089-04", "marketing_start_date": "19701209"}], "brand_name": "Dextrose and Sodium Chloride", "product_id": "0338-0089_b4404498-6ab7-4c25-a5a2-5377a6dfecca", "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": "0338-0089", "generic_name": "Dextrose and Sodium Chloride", "labeler_name": "Baxter Healthcare 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": "900 mg/100mL"}], "application_number": "NDA016678", "marketing_category": "NDA", "marketing_start_date": "19701209", "listing_expiration_date": "20261231"}