potassium chloride in sodium chloride

Generic: potassium chloride and sodium chloride

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

Drug Facts

Product Profile

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

potassium chloride 150 mg/100mL, sodium chloride 450 mg/100mL

Manufacturer
Baxter Healthcare Company

Identifiers & Regulatory

Product NDC 0338-0704
Product ID 0338-0704_0770d1c7-920a-4569-9e1d-de264bea58b1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA017648
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 03380704
Hyphenated Format 0338-0704

Supplemental Identifiers

RxCUI
237367 403890 637551
UNII
660YQ98I10 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 potassium chloride in sodium chloride (source: ndc)
Generic Name potassium chloride and sodium chloride (source: ndc)
Application Number NDA017648 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 150 mg/100mL
  • 450 mg/100mL
source: ndc
Packaging
  • 14 BAG in 1 CARTON (0338-0704-34) / 1000 mL in 1 BAG
source: ndc

Packages (1)

0338-0704-34 14 BAG in 1 CARTON (0338-0704-34) / 1000 mL in 1 BAG

Ingredients (2)

potassium chloride (150 mg/100mL) sodium chloride (450 mg/100mL)

Linked Drug Pages (1)

Potassium Chloride in Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0770d1c7-920a-4569-9e1d-de264bea58b1", "openfda": {"unii": ["660YQ98I10", "451W47IQ8X"], "rxcui": ["237367", "403890", "637551"], "spl_set_id": ["becc7410-0a25-49f5-b0c3-240078479dc8"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BAG in 1 CARTON (0338-0704-34)  / 1000 mL in 1 BAG", "package_ndc": "0338-0704-34", "marketing_start_date": "19790202"}], "brand_name": "Potassium Chloride in Sodium Chloride", "product_id": "0338-0704_0770d1c7-920a-4569-9e1d-de264bea58b1", "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": "0338-0704", "generic_name": "Potassium Chloride and Sodium Chloride", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Sodium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "150 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "450 mg/100mL"}], "application_number": "NDA017648", "marketing_category": "NDA", "marketing_start_date": "19790202", "listing_expiration_date": "20261231"}