Package 72162-1758-1

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 72162-1758-1
Digits Only 7216217581
Product NDC 72162-1758
Product ID 72162-1758_fd16299b-fcdc-4f7f-b8d4-da57f940697e
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1758-1)

Marketing

Marketing Status
Marketed Since 2024-02-07
Brand potassium citrate
Generic potassium citrate
Sample Package No

Linked Drug Pages (1)

Potassium Citrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fd16299b-fcdc-4f7f-b8d4-da57f940697e", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199381"], "spl_set_id": ["595343aa-b760-4158-9c49-dd5368f45e2c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1758-1)", "package_ndc": "72162-1758-1", "marketing_start_date": "20240207"}], "brand_name": "Potassium Citrate", "product_id": "72162-1758_fd16299b-fcdc-4f7f-b8d4-da57f940697e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "72162-1758", "generic_name": "Potassium Citrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "ANDA212779", "marketing_category": "ANDA", "marketing_start_date": "20200316", "listing_expiration_date": "20261231"}