potassium chloride er

Generic: potassium chloride er

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride er
Generic Name potassium chloride er
Labeler direct_rx
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-648
Product ID 72189-648_44821394-e7a8-de9d-e063-6294a90a97b9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214452
Listing Expiration 2026-12-31
Marketing Start 2025-11-04

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 72189648
Hyphenated Format 72189-648

Supplemental Identifiers

RxCUI
1801298
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 er (source: ndc)
Generic Name potassium chloride er (source: ndc)
Application Number ANDA214452 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-04)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-30)
source: ndc

Packages (2)

72189-648-04 4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-04) 72189-648-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-30)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Potassium Chloride ER ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "44821394-e7a8-de9d-e063-6294a90a97b9", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["42c92fcc-21d2-d32a-e063-6294a90a8312"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-04)", "package_ndc": "72189-648-04", "marketing_start_date": "20251104"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-30)", "package_ndc": "72189-648-30", "marketing_start_date": "20251104"}], "brand_name": "Potassium Chloride ER", "product_id": "72189-648_44821394-e7a8-de9d-e063-6294a90a97b9", "dosage_form": "TABLET, 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": "72189-648", "generic_name": "Potassium Chloride ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride ER", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20251104", "listing_expiration_date": "20261231"}