potassium chloride extended-release

Generic: potassium chloride extended-release

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride extended-release
Generic Name potassium chloride extended-release
Labeler bluepoint laboratories
Dosage Form TABLET
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Bluepoint Laboratories

Identifiers & Regulatory

Product NDC 68001-566
Product ID 68001-566_4341146a-910b-db91-e063-6394a90af245
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214452
Listing Expiration 2026-12-31
Marketing Start 2021-01-30

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 68001566
Hyphenated Format 68001-566

Supplemental Identifiers

RxCUI
1801294 1801298
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 extended-release (source: ndc)
Generic Name potassium chloride extended-release (source: ndc)
Application Number ANDA214452 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68001-566-00)
  • 500 TABLET in 1 BOTTLE (68001-566-03)
source: ndc

Packages (2)

68001-566-00 100 TABLET in 1 BOTTLE (68001-566-00) 68001-566-03 500 TABLET in 1 BOTTLE (68001-566-03)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Potassium Chloride Extended-release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4341146a-910b-db91-e063-6394a90af245", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["d605ca36-2bfa-42cb-a46c-8ecb3162994e"], "manufacturer_name": ["Bluepoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-566-00)", "package_ndc": "68001-566-00", "marketing_start_date": "20230417"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68001-566-03)", "package_ndc": "68001-566-03", "marketing_start_date": "20230417"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "68001-566_4341146a-910b-db91-e063-6394a90af245", "dosage_form": "TABLET", "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": "68001-566", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "Bluepoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20210130", "listing_expiration_date": "20261231"}