potassium chloride extended-release (24979-231)

Drug Facts

Product Profile

Brand Name potassium chloride extended-release

Generic Name potassium chloride

Labeler upsher-smith laboratories, llc

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

potassium chloride 750 mg/1

Manufacturer

Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 24979-231

Product ID 24979-231_70a9e07c-81ba-42a4-ae82-5f0125673744

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA209688

Listing Expiration 2026-12-31

Marketing Start 2023-04-10

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 24979231

Hyphenated Format 24979-231

Supplemental Identifiers

RxCUI

198116 628953

UPC

0324979231020 0324979231013 0324979232010

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 extended-release (source: ndc)

Generic Name potassium chloride (source: ndc)

Application Number ANDA209688 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

750 mg/1

source: ndc

Packaging

100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-01)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-02)
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-03)

source: ndc

Packages (3)

24979-231-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-01) 24979-231-02 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-02) 24979-231-03 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-03)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Potassium Chloride Extended-Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "70a9e07c-81ba-42a4-ae82-5f0125673744", "openfda": {"upc": ["0324979231020", "0324979231013", "0324979232010"], "unii": ["660YQ98I10"], "rxcui": ["198116", "628953"], "spl_set_id": ["02707146-331f-4511-a187-0152fc8bca85"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-01)", "package_ndc": "24979-231-01", "marketing_start_date": "20230410"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-02)", "package_ndc": "24979-231-02", "marketing_start_date": "20230410"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-03)", "package_ndc": "24979-231-03", "marketing_start_date": "20230410"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "24979-231_70a9e07c-81ba-42a4-ae82-5f0125673744", "dosage_form": "TABLET, 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": "24979-231", "generic_name": "Potassium Chloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA209688", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}