potassium chloride

Generic: potassium chloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler aurobindo pharma limited
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 40 meq/15mL

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-960
Product ID 59651-960_b17d54ca-5885-48d3-96e9-b29ad14f8d76
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216536
Listing Expiration 2026-12-31
Marketing Start 2025-11-20

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 59651960
Hyphenated Format 59651-960

Supplemental Identifiers

RxCUI
312515 314182
UPC
0359651959473 0359651960479
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 ANDA216536 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 meq/15mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (59651-960-47)
source: ndc

Packages (1)

59651-960-47 473 mL in 1 BOTTLE (59651-960-47)

Ingredients (1)

potassium chloride (40 meq/15mL)

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b17d54ca-5885-48d3-96e9-b29ad14f8d76", "openfda": {"upc": ["0359651959473", "0359651960479"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["b17d54ca-5885-48d3-96e9-b29ad14f8d76"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (59651-960-47)", "package_ndc": "59651-960-47", "marketing_start_date": "20251120"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "59651-960_b17d54ca-5885-48d3-96e9-b29ad14f8d76", "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": "59651-960", "generic_name": "Potassium Chloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "40 meq/15mL"}], "application_number": "ANDA216536", "marketing_category": "ANDA", "marketing_start_date": "20251120", "listing_expiration_date": "20261231"}