potassium chloride extended release
Generic: potassium chloride
Labeler: cardinal health 107, llcDrug Facts
Product Profile
Brand Name
potassium chloride extended release
Generic Name
potassium chloride
Labeler
cardinal health 107, llc
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
potassium chloride 10 meq/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
551546709
Hyphenated Format
55154-6709
Supplemental Identifiers
RxCUI
UPC
UNII
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
source: ndc
Resolved Composition
Strengths
- 10 meq/1
Packaging
- 10 BLISTER PACK in 1 BAG (55154-6709-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Packages (1)
Ingredients (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"}