Package 16571-865-01

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 16571-865-01
Digits Only 1657186501
Product NDC 16571-865
Product ID 16571-865_2e4e8acc-d3ad-4246-bd65-d95691896fc8
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-865-01)

Marketing

Marketing Status
Marketed Since 2024-12-15
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": "2e4e8acc-d3ad-4246-bd65-d95691896fc8", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381"], "spl_set_id": ["164d9d05-fbb1-4d99-8ba3-ff9c172aa8ca"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-865-01)", "package_ndc": "16571-865-01", "marketing_start_date": "20241215"}], "brand_name": "POTASSIUM CITRATE", "product_id": "16571-865_2e4e8acc-d3ad-4246-bd65-d95691896fc8", "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": "16571-865", "generic_name": "potassium citrate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CITRATE", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "1080 mg/1"}], "application_number": "ANDA077440", "marketing_category": "ANDA", "marketing_start_date": "20241215", "listing_expiration_date": "20271231"}