potassium chloride in dextrose

Generic: potassium chloride and dextrose monohydrate

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

Drug Facts

Product Profile

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

dextrose monohydrate 5 g/100mL, potassium chloride 150 mg/100mL

Manufacturer
Baxter Healthcare Company

Identifiers & Regulatory

Product NDC 0338-0683
Product ID 0338-0683_b312752a-f970-43c1-96de-eccf5a461e88
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA017634
Listing Expiration 2026-12-31
Marketing Start 1979-02-01

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03380683
Hyphenated Format 0338-0683

Supplemental Identifiers

RxCUI
309783
UNII
LX22YL083G 660YQ98I10

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 potassium chloride in dextrose (source: ndc)
Generic Name potassium chloride and dextrose monohydrate (source: ndc)
Application Number NDA017634 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • 150 mg/100mL
source: ndc
Packaging
  • 1000 mL in 1 BAG (0338-0683-04)
source: ndc

Packages (1)

0338-0683-04 1000 mL in 1 BAG (0338-0683-04)

Ingredients (2)

dextrose monohydrate (5 g/100mL) potassium chloride (150 mg/100mL)

Linked Drug Pages (1)

Potassium Chloride in Dextrose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "b312752a-f970-43c1-96de-eccf5a461e88", "openfda": {"unii": ["LX22YL083G", "660YQ98I10"], "rxcui": ["309783"], "spl_set_id": ["45de5402-5e61-4bbd-8bbc-5e3392c9920e"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BAG (0338-0683-04)", "package_ndc": "0338-0683-04", "marketing_start_date": "19790201"}], "brand_name": "Potassium Chloride in Dextrose", "product_id": "0338-0683_b312752a-f970-43c1-96de-eccf5a461e88", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0338-0683", "generic_name": "Potassium Chloride and Dextrose Monohydrate", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "150 mg/100mL"}], "application_number": "NDA017634", "marketing_category": "NDA", "marketing_start_date": "19790201", "listing_expiration_date": "20261231"}