potassium chloride
Generic: potassium chloride
Labeler: apotex corpDrug Facts
Product Profile
Brand Name
potassium chloride
Generic Name
potassium chloride
Labeler
apotex corp
Dosage Form
SOLUTION
Routes
Active Ingredients
potassium chloride 20 meq/15mL
Manufacturer
Identifiers & Regulatory
Product NDC
60505-6184
Product ID
60505-6184_d3d5d2cb-1d8d-8e62-6384-3909cae3759c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211067
Marketing Start
2021-10-07
Marketing End
2026-04-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
605056184
Hyphenated Format
60505-6184
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA211067 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 meq/15mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (60505-6184-6) / 473 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d3d5d2cb-1d8d-8e62-6384-3909cae3759c", "openfda": {"upc": ["0360505618460", "0360505618569"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["18ab4157-e99a-bff3-9ef8-9bb5c32ca36b"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (60505-6184-6) / 473 mL in 1 BOTTLE, PLASTIC", "package_ndc": "60505-6184-6", "marketing_end_date": "20260430", "marketing_start_date": "20211007"}], "brand_name": "Potassium Chloride", "product_id": "60505-6184_d3d5d2cb-1d8d-8e62-6384-3909cae3759c", "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": "60505-6184", "generic_name": "Potassium Chloride", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "ANDA211067", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20211007"}