Package 44523-410-01

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 44523-410-01
Digits Only 4452341001
Product NDC 44523-410
Product ID 44523-410_461546fa-70f8-dad0-e063-6394a90a4675
Description

100 TABLET in 1 BOTTLE (44523-410-01)

Marketing

Marketing Status
Marketed Since 2024-12-03
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": "461546fa-70f8-dad0-e063-6394a90a4675", "openfda": {"upc": ["0344523410015", "0344523415010"], "unii": ["EE90ONI6FF"], "rxcui": ["199381", "898490"], "spl_set_id": ["b32fe71a-4a58-04a1-64d3-bc3cc4a895bf"], "manufacturer_name": ["Biocomp Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (44523-410-01)", "package_ndc": "44523-410-01", "marketing_start_date": "20241203"}], "brand_name": "Potassium Citrate", "product_id": "44523-410_461546fa-70f8-dad0-e063-6394a90a4675", "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": "44523-410", "generic_name": "potassium citrate", "labeler_name": "Biocomp Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "NDA019071", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20241203", "listing_expiration_date": "20261231"}