Package 0603-1542-58

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 0603-1542-58
Digits Only 0603154258
Product NDC 0603-1542
Product ID 0603-1542_f57f6d4a-b7d8-407b-8259-19dff55a841d
Description

473 mL in 1 BOTTLE, PLASTIC (0603-1542-58)

Marketing

Marketing Status
Discontinued 2026-09-30
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f57f6d4a-b7d8-407b-8259-19dff55a841d", "openfda": {"upc": ["0306031543586", "0306031542589"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["e5214432-3517-4a90-9412-036752bd1139"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (0603-1542-58)", "package_ndc": "0603-1542-58", "marketing_end_date": "20260930", "marketing_start_date": "20150504"}], "brand_name": "Potassium Chloride", "product_id": "0603-1542_f57f6d4a-b7d8-407b-8259-19dff55a841d", "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": "0603-1542", "generic_name": "Potassium Chloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "NDA206814", "marketing_category": "NDA", "marketing_end_date": "20260930", "marketing_start_date": "20150504"}