Package 82804-075-03

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 82804-075-03
Digits Only 8280407503
Product NDC 82804-075
Product ID 82804-075_61daa681-05a0-4b2f-a6d0-c6fc1044f521
Description

3 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-03)

Marketing

Marketing Status
Marketed Since 2024-02-12
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "61daa681-05a0-4b2f-a6d0-c6fc1044f521", "openfda": {"upc": ["0382804075065"], "unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["61daa681-05a0-4b2f-a6d0-c6fc1044f521"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-03)", "package_ndc": "82804-075-03", "marketing_start_date": "20240212"}, {"sample": false, "description": "6 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-06)", "package_ndc": "82804-075-06", "marketing_start_date": "20240212"}, {"sample": false, "description": "10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-10)", "package_ndc": "82804-075-10", "marketing_start_date": "20240212"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-30)", "package_ndc": "82804-075-30", "marketing_start_date": "20240212"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-60)", "package_ndc": "82804-075-60", "marketing_start_date": "20240212"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-90)", "package_ndc": "82804-075-90", "marketing_start_date": "20240212"}], "brand_name": "Potassium Chloride", "product_id": "82804-075_61daa681-05a0-4b2f-a6d0-c6fc1044f521", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "82804-075", "generic_name": "Potassium Chloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/1"}], "application_number": "ANDA075604", "marketing_category": "ANDA", "marketing_start_date": "20020410", "listing_expiration_date": "20261231"}