Package 70518-3160-0

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 70518-3160-0
Digits Only 7051831600
Product NDC 70518-3160
Product ID 70518-3160_3a2197af-72ec-2a5e-e063-6394a90aed27
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3160-0)

Marketing

Marketing Status
Marketed Since 2021-07-15
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": "3a2197af-72ec-2a5e-e063-6394a90aed27", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199381"], "spl_set_id": ["a9cc636d-3e26-450c-9df8-665d530d626f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3160-0)", "package_ndc": "70518-3160-0", "marketing_start_date": "20210715"}], "brand_name": "Potassium Citrate", "product_id": "70518-3160_3a2197af-72ec-2a5e-e063-6394a90aed27", "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": "70518-3160", "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": "ANDA212779", "marketing_category": "ANDA", "marketing_start_date": "20210715", "listing_expiration_date": "20261231"}