potassium chloride

Generic: potassium chloride

Labeler: nexus pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler nexus pharmaceuticals llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

potassium chloride 149 mg/mL

Manufacturer
Nexus Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 14789-136
Product ID 14789-136_0ce97a26-ec41-4c7a-8198-4850a9dc81f7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217704
Listing Expiration 2026-12-31
Marketing Start 2023-09-12

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 14789136
Hyphenated Format 14789-136

Supplemental Identifiers

RxCUI
1860136 1860139
UPC
0314789136059
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 ANDA217704 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 149 mg/mL
source: ndc
Packaging
  • 25 VIAL, GLASS in 1 CARTON (14789-136-05) / 10 mL in 1 VIAL, GLASS (14789-136-07)
source: ndc

Packages (1)

14789-136-05 25 VIAL, GLASS in 1 CARTON (14789-136-05) / 10 mL in 1 VIAL, GLASS (14789-136-07)

Ingredients (1)

potassium chloride (149 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": "0ce97a26-ec41-4c7a-8198-4850a9dc81f7", "openfda": {"upc": ["0314789136059"], "unii": ["660YQ98I10"], "rxcui": ["1860136", "1860139"], "spl_set_id": ["8281fd53-f77b-42b1-9b90-449a504f5550"], "manufacturer_name": ["Nexus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, GLASS in 1 CARTON (14789-136-05)  / 10 mL in 1 VIAL, GLASS (14789-136-07)", "package_ndc": "14789-136-05", "marketing_start_date": "20230912"}], "brand_name": "Potassium Chloride", "product_id": "14789-136_0ce97a26-ec41-4c7a-8198-4850a9dc81f7", "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": "14789-136", "generic_name": "Potassium Chloride", "labeler_name": "Nexus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "149 mg/mL"}], "application_number": "ANDA217704", "marketing_category": "ANDA", "marketing_start_date": "20230912", "listing_expiration_date": "20261231"}