Package 59651-959-47

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 59651-959-47
Digits Only 5965195947
Product NDC 59651-959
Description

473 mL in 1 BOTTLE (59651-959-47)

Marketing

Marketing Status
Marketed Since 2025-11-20
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b17d54ca-5885-48d3-96e9-b29ad14f8d76", "openfda": {"upc": ["0359651959473", "0359651960479"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["b17d54ca-5885-48d3-96e9-b29ad14f8d76"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (59651-959-47)", "package_ndc": "59651-959-47", "marketing_start_date": "20251120"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "59651-959_b17d54ca-5885-48d3-96e9-b29ad14f8d76", "dosage_form": "SOLUTION", "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": "59651-959", "generic_name": "Potassium Chloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "ANDA216536", "marketing_category": "ANDA", "marketing_start_date": "20251120", "listing_expiration_date": "20261231"}