Package 62559-292-01

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 62559-292-01
Digits Only 6255929201
Product NDC 62559-292
Product ID 62559-292_ce0ee9e0-f0bc-4578-b4cd-d3d353171e82
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62559-292-01)

Marketing

Marketing Status
Marketed Since 2020-03-16
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": "ce0ee9e0-f0bc-4578-b4cd-d3d353171e82", "openfda": {"upc": ["0362559291019", "0362559292016"], "unii": ["EE90ONI6FF"], "rxcui": ["199381", "898490"], "spl_set_id": ["2fb31727-68b1-4183-947d-00e08bf99987"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62559-292-01)", "package_ndc": "62559-292-01", "marketing_start_date": "20200316"}], "brand_name": "Potassium Citrate", "product_id": "62559-292_ce0ee9e0-f0bc-4578-b4cd-d3d353171e82", "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": "62559-292", "generic_name": "Potassium Citrate", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "15 meq/1"}], "application_number": "ANDA212779", "marketing_category": "ANDA", "marketing_start_date": "20200316", "listing_expiration_date": "20261231"}