Package 63629-1967-1

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 63629-1967-1
Digits Only 6362919671
Product NDC 63629-1967
Product ID 63629-1967_72a84600-76b3-4803-ad0d-737680420295
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1967-1)

Marketing

Marketing Status
Marketed Since 2022-02-08
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": "72a84600-76b3-4803-ad0d-737680420295", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["898490"], "spl_set_id": ["f2ab3c2e-2a6e-4698-afad-260bdf0d259e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1967-1)", "package_ndc": "63629-1967-1", "marketing_start_date": "20220208"}], "brand_name": "Potassium Citrate", "product_id": "63629-1967_72a84600-76b3-4803-ad0d-737680420295", "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": "63629-1967", "generic_name": "Potassium Citrate", "labeler_name": "Bryant Ranch Prepack", "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"}