Package 72789-503-95

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 72789-503-95
Digits Only 7278950395
Product NDC 72789-503
Product ID 72789-503_34f532a1-4ea5-4a4e-e063-6294a90a0c10
Description

1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-503-95)

Marketing

Marketing Status
Marketed Since 2025-05-12
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": "34f532a1-4ea5-4a4e-e063-6294a90a0c10", "openfda": {"upc": ["0372789503950"], "unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["c2028705-9e5b-424b-983a-1c7a71dedd74"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-503-95)", "package_ndc": "72789-503-95", "marketing_start_date": "20250512"}], "brand_name": "Potassium chloride", "product_id": "72789-503_34f532a1-4ea5-4a4e-e063-6294a90a0c10", "dosage_form": "TABLET, FILM COATED, 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": "72789-503", "generic_name": "Potassium Chloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA215725", "marketing_category": "ANDA", "marketing_start_date": "20220725", "listing_expiration_date": "20261231"}