Package 82804-187-30

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 82804-187-30
Digits Only 8280418730
Product NDC 82804-187
Product ID 82804-187_7238d1d5-23c1-44d5-98fc-20d1d4e5a8ce
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-187-30)

Marketing

Marketing Status
Marketed Since 2025-01-16
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": "7238d1d5-23c1-44d5-98fc-20d1d4e5a8ce", "openfda": {"upc": ["0382804187300"], "unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["7238d1d5-23c1-44d5-98fc-20d1d4e5a8ce"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-187-30)", "package_ndc": "82804-187-30", "marketing_start_date": "20250116"}], "brand_name": "Potassium Chloride", "product_id": "82804-187_7238d1d5-23c1-44d5-98fc-20d1d4e5a8ce", "dosage_form": "TABLET, FILM COATED, 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": "82804-187", "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": "750 mg/1"}], "application_number": "ANDA209314", "marketing_category": "ANDA", "marketing_start_date": "20230807", "listing_expiration_date": "20261231"}