Package 70518-4477-0

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 70518-4477-0
Digits Only 7051844770
Product NDC 70518-4477
Product ID 70518-4477_3e9891d0-97b9-ccd1-e063-6394a90ae2cd
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4477-0)

Marketing

Marketing Status
Marketed Since 2025-09-12
Brand potassium citrate
Generic potassium citrate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e9891d0-97b9-ccd1-e063-6394a90ae2cd", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199381"], "spl_set_id": ["08c769d4-1dc0-4130-8f9c-cddace13a79b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4477-0)", "package_ndc": "70518-4477-0", "marketing_start_date": "20250912"}], "brand_name": "POTASSIUM CITRATE", "product_id": "70518-4477_3e9891d0-97b9-ccd1-e063-6394a90ae2cd", "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": "70518-4477", "generic_name": "Potassium Citrate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CITRATE", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "ANDA214420", "marketing_category": "ANDA", "marketing_start_date": "20250912", "listing_expiration_date": "20261231"}