potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

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

potassium chloride 750 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-518
Product ID 68001-518_eb3aa568-41e1-6c36-e053-2a95a90aa33a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210921
Listing Expiration 2026-12-31
Marketing Start 2021-09-10

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 68001518
Hyphenated Format 68001-518

Supplemental Identifiers

RxCUI
628953
UPC
0368001518000
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 ANDA210921 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-00)
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-08)
source: ndc

Packages (2)

68001-518-00 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-00) 68001-518-08 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-08)

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": "eb3aa568-41e1-6c36-e053-2a95a90aa33a", "openfda": {"upc": ["0368001518000"], "unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["73c911bb-4d39-4793-acba-90ed4b0eff46"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-00)", "package_ndc": "68001-518-00", "marketing_start_date": "20210910"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-518-08)", "package_ndc": "68001-518-08", "marketing_start_date": "20210910"}], "brand_name": "Potassium Chloride", "product_id": "68001-518_eb3aa568-41e1-6c36-e053-2a95a90aa33a", "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": "68001-518", "generic_name": "Potassium Chloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20210910", "listing_expiration_date": "20261231"}