potassium chloride

Generic: potassium chloride

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler major pharmaceuticals
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7543
Product ID 0904-7543_6c080e51-4eb7-4e96-b29f-eb1cce381304
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202128
Listing Expiration 2026-12-31
Marketing Start 2025-09-18

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 09047543
Hyphenated Format 0904-7543

Supplemental Identifiers

RxCUI
312504
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 ANDA202128 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7543-61) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7543-61 100 BLISTER PACK in 1 CARTON (0904-7543-61) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

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": "6c080e51-4eb7-4e96-b29f-eb1cce381304", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312504"], "spl_set_id": ["6c080e51-4eb7-4e96-b29f-eb1cce381304"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7543-61)  / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-7543-61", "marketing_start_date": "20250918"}], "brand_name": "Potassium Chloride", "product_id": "0904-7543_6c080e51-4eb7-4e96-b29f-eb1cce381304", "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": "0904-7543", "generic_name": "Potassium Chloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA202128", "marketing_category": "ANDA", "marketing_start_date": "20250918", "listing_expiration_date": "20261231"}