Package 42543-408-01

Brand: potassium citrate extended release

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 42543-408-01
Digits Only 4254340801
Product NDC 42543-408
Description

100 TABLET in 1 BOTTLE (42543-408-01)

Marketing

Marketing Status
Marketed Since 2017-11-01
Brand potassium citrate extended release
Generic potassium citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "67ba2683-6fb5-429e-ab39-6f004ac33f1b", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381", "898490"], "spl_set_id": ["5f38b02c-703c-4fc2-b833-654e41bd617f"], "manufacturer_name": ["Strides Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42543-408-01)", "package_ndc": "42543-408-01", "marketing_start_date": "20171101"}], "brand_name": "POTASSIUM CITRATE EXTENDED RELEASE", "product_id": "42543-408_67ba2683-6fb5-429e-ab39-6f004ac33f1b", "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": "42543-408", "generic_name": "POTASSIUM CITRATE", "labeler_name": "Strides Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CITRATE", "brand_name_suffix": "EXTENDED RELEASE", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "15 meq/1"}], "application_number": "ANDA206813", "marketing_category": "ANDA", "marketing_start_date": "20171101", "listing_expiration_date": "20261231"}