klor-con

Generic: potassium chloride

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name klor-con
Generic Name potassium chloride
Labeler upsher-smith laboratories, llc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 0245-0836
Product ID 0245-0836_ad0ecaea-8b55-4e39-a7ae-f7df5f206258
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218979
Listing Expiration 2026-12-31
Marketing Start 2025-08-15

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 02450836
Hyphenated Format 0245-0836

Supplemental Identifiers

RxCUI
312529 628953 628958 832718
UPC
0302450835110
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 klor-con (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA218979 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0836-11)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0836-15)
source: ndc

Packages (2)

0245-0836-11 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0836-11) 0245-0836-15 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0836-15)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

KLOR-CON ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ad0ecaea-8b55-4e39-a7ae-f7df5f206258", "openfda": {"upc": ["0302450835110"], "unii": ["660YQ98I10"], "rxcui": ["312529", "628953", "628958", "832718"], "spl_set_id": ["4340c3f2-ecf8-44cd-9b69-217f543e24e2"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0836-11)", "package_ndc": "0245-0836-11", "marketing_start_date": "20250815"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-0836-15)", "package_ndc": "0245-0836-15", "marketing_start_date": "20250815"}], "brand_name": "KLOR-CON", "product_id": "0245-0836_ad0ecaea-8b55-4e39-a7ae-f7df5f206258", "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": "0245-0836", "generic_name": "potassium chloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KLOR-CON", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA218979", "marketing_category": "ANDA", "marketing_start_date": "20250815", "listing_expiration_date": "20261231"}