Package 0591-2682-01

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 0591-2682-01
Digits Only 0591268201
Product NDC 0591-2682
Product ID 0591-2682_b81078a3-490a-4a03-a9a5-9c64acde67bf
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0591-2682-01)

Marketing

Marketing Status
Marketed Since 2018-05-30
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": "b81078a3-490a-4a03-a9a5-9c64acde67bf", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381", "898490"], "spl_set_id": ["ac173781-486b-461c-97ae-8b5c69e20792"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0591-2682-01)", "package_ndc": "0591-2682-01", "marketing_start_date": "20180530"}], "brand_name": "Potassium Citrate", "product_id": "0591-2682_b81078a3-490a-4a03-a9a5-9c64acde67bf", "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": "0591-2682", "generic_name": "Potassium Citrate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "5 meq/1"}], "application_number": "ANDA209758", "marketing_category": "ANDA", "marketing_start_date": "20180530", "listing_expiration_date": "20261231"}