Package 50090-7616-0

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 50090-7616-0
Digits Only 5009076160
Product NDC 50090-7616
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7616-0)

Marketing

Marketing Status
Marketed Since 2025-07-29
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4fe715ed-5979-44d7-85b7-46d3080ec473", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["162a8ab5-76cf-48fa-8487-7780ed65647e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7616-0)", "package_ndc": "50090-7616-0", "marketing_start_date": "20250729"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "50090-7616_4fe715ed-5979-44d7-85b7-46d3080ec473", "dosage_form": "TABLET, 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": "50090-7616", "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": "1500 mg/1"}], "application_number": "ANDA214422", "marketing_category": "ANDA", "marketing_start_date": "20210120", "listing_expiration_date": "20261231"}