potassium chloride

Generic: potassium chloride

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 1500 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8580
Product ID 0615-8580_6a988bea-a4e8-4d1c-9a04-429932c1fa4a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212561
Listing Expiration 2026-12-31
Marketing Start 2020-02-01

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 06158580
Hyphenated Format 0615-8580

Supplemental Identifiers

RxCUI
198116
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 ANDA212561 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1500 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8580-05)
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8580-39)
source: ndc

Packages (2)

0615-8580-05 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8580-05) 0615-8580-39 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8580-39)

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": "6a988bea-a4e8-4d1c-9a04-429932c1fa4a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["198116"], "spl_set_id": ["542e16b0-44db-490f-b44e-4c88a6e3d8b8"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8580-05)", "package_ndc": "0615-8580-05", "marketing_start_date": "20250916"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8580-39)", "package_ndc": "0615-8580-39", "marketing_start_date": "20250916"}], "brand_name": "Potassium Chloride", "product_id": "0615-8580_6a988bea-a4e8-4d1c-9a04-429932c1fa4a", "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": "0615-8580", "generic_name": "Potassium Chloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA212561", "marketing_category": "ANDA", "marketing_start_date": "20200201", "listing_expiration_date": "20261231"}