potassium chloride

Generic: potassium chloride

Labeler: nexus pharamaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler nexus pharamaceuticals inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

potassium chloride 7.45 mg/mL

Manufacturer
Nexus Pharamaceuticals Inc.

Identifiers & Regulatory

Product NDC 14789-109
Product ID 14789-109_fd507baf-f17a-4294-af56-ca6a5052cb1e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214727
Listing Expiration 2026-12-31
Marketing Start 2021-02-28

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 14789109
Hyphenated Format 14789-109

Supplemental Identifiers

RxCUI
312507 1860239 1860241 1860463 1860466
UPC
0314789107165 0314789107080 0314789109169 0314789108162 0314789108087
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 ANDA214727 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 7.45 mg/mL
source: ndc
Packaging
  • 24 BAG in 1 BOX (14789-109-10) / 100 mL in 1 BAG (14789-109-16)
source: ndc

Packages (1)

14789-109-10 24 BAG in 1 BOX (14789-109-10) / 100 mL in 1 BAG (14789-109-16)

Ingredients (1)

potassium chloride (7.45 mg/mL)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "fd507baf-f17a-4294-af56-ca6a5052cb1e", "openfda": {"upc": ["0314789107165", "0314789107080", "0314789109169", "0314789108162", "0314789108087"], "unii": ["660YQ98I10"], "rxcui": ["312507", "1860239", "1860241", "1860463", "1860466"], "spl_set_id": ["765ef38c-df36-46d1-9062-61e30ff46a86"], "manufacturer_name": ["Nexus Pharamaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 BOX (14789-109-10)  / 100 mL in 1 BAG (14789-109-16)", "package_ndc": "14789-109-10", "marketing_start_date": "20210228"}], "brand_name": "Potassium Chloride", "product_id": "14789-109_fd507baf-f17a-4294-af56-ca6a5052cb1e", "dosage_form": "INJECTION", "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": "14789-109", "generic_name": "Potassium Chloride", "labeler_name": "Nexus Pharamaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "7.45 mg/mL"}], "application_number": "ANDA214727", "marketing_category": "ANDA", "marketing_start_date": "20210228", "listing_expiration_date": "20261231"}