potassium chloride

Generic: potassium chloride

Labeler: advagen pharma ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

potassium chloride 1125 mg/1

Manufacturer
Advagen Pharma Ltd

Identifiers & Regulatory

Product NDC 72888-201
Product ID 72888-201_43ef4dac-5602-40dc-e063-6394a90af863
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215725
Listing Expiration 2026-12-31
Marketing Start 2024-08-22

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 72888201
Hyphenated Format 72888-201

Supplemental Identifiers

RxCUI
198116 628953 2693253
UPC
0372888076058 0372888201009 0372888075006 0372888201016 0372888075051 0372888076010 0372888075013
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 ANDA215725 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1125 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-201-00)
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-201-01)
source: ndc

Packages (2)

72888-201-00 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-201-00) 72888-201-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-201-01)

Ingredients (1)

potassium chloride (1125 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": "43ef4dac-5602-40dc-e063-6394a90af863", "openfda": {"upc": ["0372888076058", "0372888201009", "0372888075006", "0372888201016", "0372888075051", "0372888076010", "0372888075013"], "unii": ["660YQ98I10"], "rxcui": ["198116", "628953", "2693253"], "spl_set_id": ["8000e242-fe20-4d02-8f7d-97298857cf4c"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-201-00)", "package_ndc": "72888-201-00", "marketing_start_date": "20240822"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-201-01)", "package_ndc": "72888-201-01", "marketing_start_date": "20240822"}], "brand_name": "Potassium chloride", "product_id": "72888-201_43ef4dac-5602-40dc-e063-6394a90af863", "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": "72888-201", "generic_name": "Potassium Chloride", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1125 mg/1"}], "application_number": "ANDA215725", "marketing_category": "ANDA", "marketing_start_date": "20240822", "listing_expiration_date": "20261231"}