Package 72865-193-01

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 72865-193-01
Digits Only 7286519301
Product NDC 72865-193
Product ID 72865-193_7809b770-e255-4e34-b38f-90a0d51eeaea
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-193-01)

Marketing

Marketing Status
Marketed Since 2021-02-25
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": "7809b770-e255-4e34-b38f-90a0d51eeaea", "openfda": {"upc": ["0372865193013", "0372865191019", "0372865192016"], "unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381", "898490"], "spl_set_id": ["360a1012-4bdb-473a-8f1f-4550d3b51343"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-193-01)", "package_ndc": "72865-193-01", "marketing_start_date": "20210225"}], "brand_name": "POTASSIUM CITRATE", "product_id": "72865-193_7809b770-e255-4e34-b38f-90a0d51eeaea", "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": "72865-193", "generic_name": "Potassium Citrate", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CITRATE", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "15 meq/1"}], "application_number": "ANDA214420", "marketing_category": "ANDA", "marketing_start_date": "20210215", "listing_expiration_date": "20261231"}