potassium chloride

Generic: potassium chloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-187
Product ID 82804-187_7238d1d5-23c1-44d5-98fc-20d1d4e5a8ce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209314
Listing Expiration 2026-12-31
Marketing Start 2023-08-07

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 82804187
Hyphenated Format 82804-187

Supplemental Identifiers

RxCUI
628953
UPC
0382804187300
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 ANDA209314 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-187-30)
source: ndc

Packages (1)

82804-187-30 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-187-30)

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": "7238d1d5-23c1-44d5-98fc-20d1d4e5a8ce", "openfda": {"upc": ["0382804187300"], "unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["7238d1d5-23c1-44d5-98fc-20d1d4e5a8ce"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-187-30)", "package_ndc": "82804-187-30", "marketing_start_date": "20250116"}], "brand_name": "Potassium Chloride", "product_id": "82804-187_7238d1d5-23c1-44d5-98fc-20d1d4e5a8ce", "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": "82804-187", "generic_name": "Potassium Chloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA209314", "marketing_category": "ANDA", "marketing_start_date": "20230807", "listing_expiration_date": "20261231"}