Package 50090-7749-0

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 50090-7749-0
Digits Only 5009077490
Product NDC 50090-7749
Product ID 50090-7749_5f624ab1-8eca-415e-9141-43ba1e6f7955
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7749-0)

Marketing

Marketing Status
Marketed Since 2025-11-03
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": "5f624ab1-8eca-415e-9141-43ba1e6f7955", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["4a2173ba-556b-4ad7-be81-4da79b739490"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7749-0)", "package_ndc": "50090-7749-0", "marketing_start_date": "20251103"}], "brand_name": "Potassium chloride", "product_id": "50090-7749_5f624ab1-8eca-415e-9141-43ba1e6f7955", "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": "50090-7749", "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": "ANDA215725", "marketing_category": "ANDA", "marketing_start_date": "20220725", "listing_expiration_date": "20261231"}