Package 68382-537-16

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 68382-537-16
Digits Only 6838253716
Product NDC 68382-537
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-16)

Marketing

Marketing Status
Marketed Since 2014-08-12
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": "b0382b88-fcc4-44de-b66d-a93dabc596f8", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199376", "199381", "898490"], "spl_set_id": ["1a839f91-9bbd-4f46-b350-c5e8074b5db7"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-01)", "package_ndc": "68382-537-01", "marketing_start_date": "20140812"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-05)", "package_ndc": "68382-537-05", "marketing_start_date": "20140812"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-06)", "package_ndc": "68382-537-06", "marketing_start_date": "20140812"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-10)", "package_ndc": "68382-537-10", "marketing_start_date": "20140812"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-16)", "package_ndc": "68382-537-16", "marketing_start_date": "20140812"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-537-30)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "68382-537-30", "marketing_start_date": "20140812"}], "brand_name": "Potassium Citrate", "product_id": "68382-537_b0382b88-fcc4-44de-b66d-a93dabc596f8", "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": "68382-537", "generic_name": "Potassium Citrate", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "ANDA203546", "marketing_category": "ANDA", "marketing_start_date": "20140812", "listing_expiration_date": "20261231"}