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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 20 meq/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-075
Product ID 82804-075_61daa681-05a0-4b2f-a6d0-c6fc1044f521
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075604
Listing Expiration 2026-12-31
Marketing Start 2002-04-10

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 82804075
Hyphenated Format 82804-075

Supplemental Identifiers

RxCUI
1801294
UPC
0382804075065
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 ANDA075604 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 meq/1
source: ndc
Packaging
  • 3 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-03)
  • 6 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-06)
  • 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-10)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-90)
source: ndc

Packages (6)

82804-075-03 3 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-03) 82804-075-06 6 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-06) 82804-075-10 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-10) 82804-075-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-30) 82804-075-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-60) 82804-075-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-90)

Ingredients (1)

potassium chloride (20 meq/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": "61daa681-05a0-4b2f-a6d0-c6fc1044f521", "openfda": {"upc": ["0382804075065"], "unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["61daa681-05a0-4b2f-a6d0-c6fc1044f521"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-03)", "package_ndc": "82804-075-03", "marketing_start_date": "20240212"}, {"sample": false, "description": "6 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-06)", "package_ndc": "82804-075-06", "marketing_start_date": "20240212"}, {"sample": false, "description": "10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-10)", "package_ndc": "82804-075-10", "marketing_start_date": "20240212"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-30)", "package_ndc": "82804-075-30", "marketing_start_date": "20240212"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-60)", "package_ndc": "82804-075-60", "marketing_start_date": "20240212"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-90)", "package_ndc": "82804-075-90", "marketing_start_date": "20240212"}], "brand_name": "Potassium Chloride", "product_id": "82804-075_61daa681-05a0-4b2f-a6d0-c6fc1044f521", "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": "82804-075", "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": "20 meq/1"}], "application_number": "ANDA075604", "marketing_category": "ANDA", "marketing_start_date": "20020410", "listing_expiration_date": "20261231"}