Package 0245-0070-11

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 0245-0070-11
Digits Only 0245007011
Product NDC 0245-0070
Description

100 TABLET in 1 BOTTLE (0245-0070-11)

Marketing

Marketing Status
Discontinued 2027-07-31
Brand potassium citrate
Generic potassium citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39e81850-ac5b-656e-e063-6294a90a1d94", "openfda": {"upc": ["0302450071112"], "unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381"], "spl_set_id": ["2215dc1d-0b5a-469e-9b51-4d7480a51078"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0245-0070-11)", "package_ndc": "0245-0070-11", "marketing_end_date": "20270731", "marketing_start_date": "20060901"}], "brand_name": "Potassium Citrate", "product_id": "0245-0070_39e81850-ac5b-656e-e063-6294a90a1d94", "dosage_form": "TABLET", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "0245-0070", "generic_name": "potassium citrate", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "5 meq/1"}], "application_number": "NDA019071", "marketing_category": "NDA", "marketing_end_date": "20270731", "marketing_start_date": "20060901"}