Package 0904-7543-61

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 0904-7543-61
Digits Only 0904754361
Product NDC 0904-7543
Product ID 0904-7543_6c080e51-4eb7-4e96-b29f-eb1cce381304
Description

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

Marketing

Marketing Status
Marketed Since 2025-09-18
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": "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"}