Package 50090-7616-0
Brand: potassium chloride
Generic: potassium chloridePackage 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
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"}