Package 72162-2122-1

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 72162-2122-1
Digits Only 7216221221
Product NDC 72162-2122
Product ID 72162-2122_4ee28ca5-549e-4bcf-b77f-9fe341a6631b
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2122-1)

Marketing

Marketing Status
Marketed Since 2023-09-18
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": "4ee28ca5-549e-4bcf-b77f-9fe341a6631b", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199376"], "spl_set_id": ["b977c77b-c212-408e-adac-61736e5ed362"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2122-1)", "package_ndc": "72162-2122-1", "marketing_start_date": "20230918"}], "brand_name": "POTASSIUM CITRATE", "product_id": "72162-2122_4ee28ca5-549e-4bcf-b77f-9fe341a6631b", "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": "72162-2122", "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": "5 meq/1"}], "application_number": "ANDA214420", "marketing_category": "ANDA", "marketing_start_date": "20210215", "listing_expiration_date": "20261231"}