potassium chloride

Generic: potassium chloride

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

potassium chloride 750 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-027
Product ID 72189-027_2c4e994c-a009-5fc9-e063-6294a90a462a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210733
Listing Expiration 2026-12-31
Marketing Start 2019-10-02

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 72189027
Hyphenated Format 72189-027

Supplemental Identifiers

RxCUI
628953
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 ANDA210733 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-04)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-30)
source: ndc

Packages (2)

72189-027-04 4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-04) 72189-027-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-30)

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": "2c4e994c-a009-5fc9-e063-6294a90a462a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["946b9568-671d-172a-e053-2a95a90ac827"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-04)", "package_ndc": "72189-027-04", "marketing_start_date": "20191002"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-027-30)", "package_ndc": "72189-027-30", "marketing_start_date": "20191002"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "72189-027_2c4e994c-a009-5fc9-e063-6294a90a462a", "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": "72189-027", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA210733", "marketing_category": "ANDA", "marketing_start_date": "20191002", "listing_expiration_date": "20261231"}