potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler baxter healthcare corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

potassium chloride 29.8 g/1000mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-0703
Product ID 0338-0703_4cf18d0e-1854-48fb-b711-49b2a3042ae4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019904
Listing Expiration 2027-12-31
Marketing Start 1989-12-26

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 03380703
Hyphenated Format 0338-0703

Supplemental Identifiers

RxCUI
312507 1860239 1860241 1860463 1860466
UNII
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 (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number NDA019904 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 29.8 g/1000mL
source: ndc
Packaging
  • 24 BAG in 1 CARTON (0338-0703-41) / 50 mL in 1 BAG
  • 24 BAG in 1 CARTON (0338-0703-48) / 100 mL in 1 BAG
source: ndc

Packages (2)

0338-0703-41 24 BAG in 1 CARTON (0338-0703-41) / 50 mL in 1 BAG 0338-0703-48 24 BAG in 1 CARTON (0338-0703-48) / 100 mL in 1 BAG

Ingredients (1)

potassium chloride (29.8 g/1000mL)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "4cf18d0e-1854-48fb-b711-49b2a3042ae4", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312507", "1860239", "1860241", "1860463", "1860466"], "spl_set_id": ["092ddee4-572d-4771-8d95-880cea01097e"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CARTON (0338-0703-41)  / 50 mL in 1 BAG", "package_ndc": "0338-0703-41", "marketing_start_date": "19891226"}, {"sample": false, "description": "24 BAG in 1 CARTON (0338-0703-48)  / 100 mL in 1 BAG", "package_ndc": "0338-0703-48", "marketing_start_date": "19891226"}], "brand_name": "Potassium Chloride", "product_id": "0338-0703_4cf18d0e-1854-48fb-b711-49b2a3042ae4", "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": "0338-0703", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "29.8 g/1000mL"}], "application_number": "NDA019904", "marketing_category": "NDA", "marketing_start_date": "19891226", "listing_expiration_date": "20271231"}