potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler solco healthcare llc
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Solco Healthcare LLC

Identifiers & Regulatory

Product NDC 43547-553
Product ID 43547-553_580cdd01-0999-41cc-a4a1-6798a71ef6d5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209026
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 43547553
Hyphenated Format 43547-553

Supplemental Identifiers

RxCUI
312504 315183
UPC
0343547553104 0343547552107
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 (source: ndc)
Application Number ANDA209026 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43547-553-10)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43547-553-50)
source: ndc

Packages (2)

43547-553-10 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43547-553-10) 43547-553-50 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43547-553-50)

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": "580cdd01-0999-41cc-a4a1-6798a71ef6d5", "openfda": {"upc": ["0343547553104", "0343547552107"], "unii": ["660YQ98I10"], "rxcui": ["312504", "315183"], "spl_set_id": ["52d91d76-8c7f-40f1-9f5c-e05962cabedd"], "manufacturer_name": ["Solco Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43547-553-10)", "package_ndc": "43547-553-10", "marketing_start_date": "20190430"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43547-553-50)", "package_ndc": "43547-553-50", "marketing_start_date": "20190430"}], "brand_name": "potassium chloride", "product_id": "43547-553_580cdd01-0999-41cc-a4a1-6798a71ef6d5", "dosage_form": "CAPSULE, 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": "43547-553", "generic_name": "potassium chloride", "labeler_name": "Solco Healthcare LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA209026", "marketing_category": "ANDA", "marketing_start_date": "20190430", "listing_expiration_date": "20261231"}