Package 50090-7640-0

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 50090-7640-0
Digits Only 5009076400
Product NDC 50090-7640
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7640-0)

Marketing

Marketing Status
Marketed Since 2025-08-26
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "065ea1f2-b00c-4315-9e47-1186d6faa911", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["8f6ea056-5e10-4de1-97f0-55f0655a6f78"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7640-0)", "package_ndc": "50090-7640-0", "marketing_start_date": "20250826"}], "brand_name": "Potassium Chloride", "product_id": "50090-7640_065ea1f2-b00c-4315-9e47-1186d6faa911", "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": "50090-7640", "generic_name": "Potassium Chloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "NDA019123", "marketing_category": "NDA", "marketing_start_date": "19860417", "listing_expiration_date": "20261231"}