potassium chloride

Generic: potassium chloride extended-release

Labeler: solco healthcare llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride extended-release
Labeler solco healthcare llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

potassium chloride 1125 mg/1

Manufacturer
Solco Healthcare LLC

Identifiers & Regulatory

Product NDC 43547-551
Product ID 43547-551_f704b746-ab75-4484-8704-5baa94a07750
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209922
Listing Expiration 2026-12-31
Marketing Start 2019-04-30

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 43547551
Hyphenated Format 43547-551

Supplemental Identifiers

RxCUI
403888 1801294 1801298
UNII
660YQ98I10

Packaging Origin

Original Packager
true

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 extended-release (source: ndc)
Application Number ANDA209922 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1125 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (43547-551-10)
source: ndc

Packages (1)

43547-551-10 100 TABLET in 1 BOTTLE (43547-551-10)

Ingredients (1)

potassium chloride (1125 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": "f704b746-ab75-4484-8704-5baa94a07750", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["403888", "1801294", "1801298"], "spl_set_id": ["f704b746-ab75-4484-8704-5baa94a07750"], "manufacturer_name": ["Solco Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43547-551-10)", "package_ndc": "43547-551-10", "marketing_start_date": "20190430"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "43547-551_f704b746-ab75-4484-8704-5baa94a07750", "dosage_form": "TABLET", "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": "43547-551", "generic_name": "potassium chloride extended-release", "labeler_name": "Solco Healthcare LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1125 mg/1"}], "application_number": "ANDA209922", "marketing_category": "ANDA", "marketing_start_date": "20190430", "listing_expiration_date": "20261231"}