potassium chloride extended release

Generic: potassium chloride

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride extended release
Generic Name potassium chloride
Labeler cardinal health 107, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 10 meq/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-6709
Product ID 55154-6709_48bda54d-9d59-46cd-bd32-fa89ef93c1b7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205993
Marketing Start 2015-12-11
Marketing End 2026-05-31

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 551546709
Hyphenated Format 55154-6709

Supplemental Identifiers

RxCUI
628953
UPC
0055154670906
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 (source: ndc)
Application Number ANDA205993 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 meq/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-6709-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

potassium chloride (10 meq/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48bda54d-9d59-46cd-bd32-fa89ef93c1b7", "openfda": {"upc": ["0055154670906"], "unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["446ad1bd-cf5c-41a7-945f-a6575cab16bf"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-6709-0)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-6709-0", "marketing_end_date": "20260531", "marketing_start_date": "20160505"}], "brand_name": "Potassium chloride extended release", "product_id": "55154-6709_48bda54d-9d59-46cd-bd32-fa89ef93c1b7", "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": "55154-6709", "generic_name": "Potassium chloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium chloride extended release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "10 meq/1"}], "application_number": "ANDA205993", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "20151211"}