potassium chloride

Generic: potassium chloride

Labeler: macleods pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler macleods pharmaceuticals limited
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 20 meq/15mL

Manufacturer
Macleods Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 33342-511
Product ID 33342-511_89d827c8-91af-4bfd-a846-62e55824e983
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218733
Listing Expiration 2026-12-31
Marketing Start 2023-05-26

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 33342511
Hyphenated Format 33342-511

Supplemental Identifiers

RxCUI
312515 314182
UPC
0333342512734
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 ANDA218733 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 meq/15mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (33342-511-73)
source: ndc

Packages (1)

Ingredients (1)

potassium chloride (20 meq/15mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "89d827c8-91af-4bfd-a846-62e55824e983", "openfda": {"upc": ["0333342512734"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["89d827c8-91af-4bfd-a846-62e55824e983"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (33342-511-73)", "package_ndc": "33342-511-73", "marketing_start_date": "20230526"}], "brand_name": "Potassium Chloride", "product_id": "33342-511_89d827c8-91af-4bfd-a846-62e55824e983", "dosage_form": "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": "33342-511", "generic_name": "Potassium Chloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "ANDA218733", "marketing_category": "ANDA", "marketing_start_date": "20230526", "listing_expiration_date": "20261231"}