potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name potassium chloride
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 0832-5323
Product ID 0832-5323_39e726b1-eab8-fcf4-e063-6394a90a950a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019123
Listing Expiration 2026-12-31
Marketing Start 1986-04-17

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 08325323
Hyphenated Format 0832-5323

Supplemental Identifiers

RxCUI
312529 628953
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 NDA019123 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-10)
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-11)
source: ndc

Packages (2)

0832-5323-10 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-10) 0832-5323-11 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-11)

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": "39e726b1-eab8-fcf4-e063-6394a90a950a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["616f0de7-8843-44a1-8fa6-274d889286aa"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-10)", "package_ndc": "0832-5323-10", "marketing_start_date": "20190621"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-11)", "package_ndc": "0832-5323-11", "marketing_start_date": "20190621"}], "brand_name": "Potassium Chloride", "product_id": "0832-5323_39e726b1-eab8-fcf4-e063-6394a90a950a", "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": "0832-5323", "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": "NDA019123", "marketing_category": "NDA", "marketing_start_date": "19860417", "listing_expiration_date": "20261231"}