Package 50090-6635-0

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 50090-6635-0
Digits Only 5009066350
Product NDC 50090-6635
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6635-0)

Marketing

Marketing Status
Marketed Since 2023-08-25
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": "95866e15-d194-4771-8617-2dcf94808d1d", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["f1af7e05-68ba-438e-a63b-cd8c23960c85"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6635-0)", "package_ndc": "50090-6635-0", "marketing_start_date": "20230825"}], "brand_name": "Potassium Chloride", "product_id": "50090-6635_95866e15-d194-4771-8617-2dcf94808d1d", "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": "50090-6635", "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": "10 meq/1"}], "application_number": "ANDA204662", "marketing_category": "ANDA", "marketing_start_date": "20161109", "listing_expiration_date": "20261231"}