Package 72162-2476-1

Brand: potassium citrate extended release

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 72162-2476-1
Digits Only 7216224761
Product NDC 72162-2476
Product ID 72162-2476_5ce2f57e-a740-4806-9605-c339b82af8d5
Description

100 TABLET in 1 BOTTLE (72162-2476-1)

Marketing

Marketing Status
Marketed Since 2025-05-01
Brand potassium citrate extended release
Generic potassium citrate
Sample Package No

Linked Drug Pages (1)

POTASSIUM CITRATE EXTENDED RELEASE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5ce2f57e-a740-4806-9605-c339b82af8d5", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199376"], "spl_set_id": ["44ab2c4f-4a76-470d-98fb-8874c692a967"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2476-1)", "package_ndc": "72162-2476-1", "marketing_start_date": "20250501"}], "brand_name": "POTASSIUM CITRATE EXTENDED RELEASE", "product_id": "72162-2476_5ce2f57e-a740-4806-9605-c339b82af8d5", "dosage_form": "TABLET", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "72162-2476", "generic_name": "POTASSIUM CITRATE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CITRATE", "brand_name_suffix": "EXTENDED RELEASE", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "5 meq/1"}], "application_number": "ANDA206813", "marketing_category": "ANDA", "marketing_start_date": "20171101", "listing_expiration_date": "20261231"}