potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler upsher-smithlaboratories, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 1500 mg/1

Manufacturer
Upsher-SmithLaboratories, LLC

Identifiers & Regulatory

Product NDC 0832-5325
Product ID 0832-5325_39990061-98d4-6669-e063-6394a90ae067
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074726
Listing Expiration 2026-12-31
Marketing Start 1998-11-20

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 08325325
Hyphenated Format 0832-5325

Supplemental Identifiers

RxCUI
1801294 1801298
UPC
0308325325113 0308325324116
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 ANDA074726 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1500 mg/1
source: ndc
Packaging
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-10)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-11)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-15)
source: ndc

Packages (3)

0832-5325-10 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-10) 0832-5325-11 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-11) 0832-5325-15 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-15)

Ingredients (1)

potassium chloride (1500 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": "39990061-98d4-6669-e063-6394a90ae067", "openfda": {"upc": ["0308325325113", "0308325324116"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["ad584ce4-a64d-4851-80e9-0eeedc0b9d06"], "manufacturer_name": ["Upsher-SmithLaboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-10)", "package_ndc": "0832-5325-10", "marketing_start_date": "20190621"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-11)", "package_ndc": "0832-5325-11", "marketing_start_date": "20190621"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-15)", "package_ndc": "0832-5325-15", "marketing_start_date": "20190621"}], "brand_name": "Potassium Chloride", "product_id": "0832-5325_39990061-98d4-6669-e063-6394a90ae067", "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": "0832-5325", "generic_name": "potassium chloride", "labeler_name": "Upsher-SmithLaboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA074726", "marketing_category": "ANDA", "marketing_start_date": "19981120", "listing_expiration_date": "20261231"}