potassium chloride in dextrose and sodium chloride

Generic: potassium chloride, dextrose monohydrate and sodium chloride

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

Drug Facts

Product Profile

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

dextrose monohydrate 5 g/100mL, potassium chloride 75 mg/100mL, sodium chloride 450 mg/100mL

Manufacturer
Baxter Healthcare Company

Identifiers & Regulatory

Product NDC 0338-0669
Product ID 0338-0669_34c74d23-f49a-4e1c-9ffe-9a200d0fffe7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018008
Listing Expiration 2026-12-31
Marketing Start 1979-02-02

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 03380669
Hyphenated Format 0338-0669

Supplemental Identifiers

RxCUI
615099 615100 615107 615111 630796 1863605 1863607 1863973 1863975 1863988
UNII
660YQ98I10 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 potassium chloride in dextrose and sodium chloride (source: ndc)
Generic Name potassium chloride, dextrose monohydrate and sodium chloride (source: ndc)
Application Number NDA018008 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • 75 mg/100mL
  • 450 mg/100mL
source: ndc
Packaging
  • 1000 mL in 1 BAG (0338-0669-04)
source: ndc

Packages (1)

0338-0669-04 1000 mL in 1 BAG (0338-0669-04)

Ingredients (3)

dextrose monohydrate (5 g/100mL) potassium chloride (75 mg/100mL) sodium chloride (450 mg/100mL)

Linked Drug Pages (1)

Potassium Chloride in Dextrose and Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "34c74d23-f49a-4e1c-9ffe-9a200d0fffe7", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X", "LX22YL083G"], "rxcui": ["615099", "615100", "615107", "615111", "630796", "1863605", "1863607", "1863973", "1863975", "1863988"], "spl_set_id": ["c553fed1-3de5-4826-8eff-633b5923bf0b"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BAG (0338-0669-04)", "package_ndc": "0338-0669-04", "marketing_start_date": "19790202"}], "brand_name": "Potassium Chloride in Dextrose and Sodium Chloride", "product_id": "0338-0669_34c74d23-f49a-4e1c-9ffe-9a200d0fffe7", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0338-0669", "generic_name": "Potassium Chloride, Dextrose Monohydrate and Sodium Chloride", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Dextrose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "75 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "450 mg/100mL"}], "application_number": "NDA018008", "marketing_category": "NDA", "marketing_start_date": "19790202", "listing_expiration_date": "20261231"}