potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name potassium chloride
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 24979-230
Product ID 24979-230_d03706f3-78e7-4be3-8f41-af67f60b0178
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218979
Listing Expiration 2026-12-31
Marketing Start 2024-10-28

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 24979230
Hyphenated Format 24979-230

Supplemental Identifiers

RxCUI
312529 628953
UPC
0324979229010 0324979230016
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 ANDA218979 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 64000 TABLET, EXTENDED RELEASE in 1 DRUM (24979-230-00)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-01)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-03)
source: ndc

Packages (3)

24979-230-00 64000 TABLET, EXTENDED RELEASE in 1 DRUM (24979-230-00) 24979-230-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-01) 24979-230-03 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-03)

Ingredients (1)

potassium chloride (750 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": "d03706f3-78e7-4be3-8f41-af67f60b0178", "openfda": {"upc": ["0324979229010", "0324979230016"], "unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["a230185f-5493-487d-892a-5219869b4e47"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "64000 TABLET, EXTENDED RELEASE in 1 DRUM (24979-230-00)", "package_ndc": "24979-230-00", "marketing_start_date": "20250601"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-01)", "package_ndc": "24979-230-01", "marketing_start_date": "20241028"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-230-03)", "package_ndc": "24979-230-03", "marketing_start_date": "20241028"}], "brand_name": "Potassium Chloride", "product_id": "24979-230_d03706f3-78e7-4be3-8f41-af67f60b0178", "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": "24979-230", "generic_name": "Potassium Chloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA218979", "marketing_category": "ANDA", "marketing_start_date": "20241028", "listing_expiration_date": "20261231"}