potassium chloride extended-release (82804-109)

Drug Facts

Product Profile

Brand Name potassium chloride extended-release

Generic Name potassium chloride extended-release

Labeler proficient rx lp

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

potassium chloride 750 mg/1

Manufacturer

Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-109

Product ID 82804-109_c53d1db5-1c9e-4289-a2a2-961e0dd56f32

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA214452

Listing Expiration 2026-12-31

Marketing Start 2021-01-30

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 82804109

Hyphenated Format 82804-109

Supplemental Identifiers

RxCUI

1801298

UPC

0382804109302

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 extended-release (source: ndc)

Generic Name potassium chloride extended-release (source: ndc)

Application Number ANDA214452 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

750 mg/1

source: ndc

Packaging

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-109-30)

source: ndc

Packages (1)

82804-109-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-109-30)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Potassium Chloride Extended-release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "c53d1db5-1c9e-4289-a2a2-961e0dd56f32", "openfda": {"upc": ["0382804109302"], "unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["c53d1db5-1c9e-4289-a2a2-961e0dd56f32"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-109-30)", "package_ndc": "82804-109-30", "marketing_start_date": "20240614"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "82804-109_c53d1db5-1c9e-4289-a2a2-961e0dd56f32", "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": "82804-109", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20210130", "listing_expiration_date": "20261231"}