potassium chloride

Generic: potassium chloride

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler avkare
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-506
Product ID 42291-506_3a9ee76a-b914-17bb-e063-6294a90aad71
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019123
Listing Expiration 2026-12-31
Marketing Start 2019-06-21

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 42291506
Hyphenated Format 42291-506

Supplemental Identifiers

RxCUI
628953
UNII
660YQ98I10

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
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-01)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-50)
source: ndc

Packages (2)

42291-506-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-01) 42291-506-50 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-50)

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": "3a9ee76a-b914-17bb-e063-6294a90aad71", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["8bb030b7-104a-373b-e053-2995a90ab580"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-01)", "package_ndc": "42291-506-01", "marketing_start_date": "20190621"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-50)", "package_ndc": "42291-506-50", "marketing_start_date": "20190621"}], "brand_name": "Potassium Chloride", "product_id": "42291-506_3a9ee76a-b914-17bb-e063-6294a90aad71", "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": "42291-506", "generic_name": "Potassium Chloride", "labeler_name": "AvKARE", "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": "20190621", "listing_expiration_date": "20261231"}