potassium chloride

Generic: potassium chloride

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler epic pharma, llc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 600 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-422
Product ID 42806-422_3f74c669-3182-952f-e063-6294a90aad92
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209314
Listing Expiration 2026-12-31
Marketing Start 2023-08-07

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 42806422
Hyphenated Format 42806-422

Supplemental Identifiers

RxCUI
312529 628953
UPC
0342806422106 0342806423103
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 ANDA209314 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-01)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-05)
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-10)
source: ndc

Packages (3)

42806-422-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-01) 42806-422-05 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-05) 42806-422-10 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-10)

Ingredients (1)

potassium chloride (600 mg/1)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f74c669-3182-952f-e063-6294a90aad92", "openfda": {"upc": ["0342806422106", "0342806423103"], "unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["00615fad-ad3b-46e8-a89d-48290d937ae2"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-01)", "package_ndc": "42806-422-01", "marketing_start_date": "20230807"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-05)", "package_ndc": "42806-422-05", "marketing_start_date": "20230807"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-10)", "package_ndc": "42806-422-10", "marketing_start_date": "20230807"}], "brand_name": "Potassium Chloride", "product_id": "42806-422_3f74c669-3182-952f-e063-6294a90aad92", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "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": "42806-422", "generic_name": "Potassium Chloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "600 mg/1"}], "application_number": "ANDA209314", "marketing_category": "ANDA", "marketing_start_date": "20230807", "listing_expiration_date": "20261231"}