Package 82804-109-30

{"route": ["ORAL"], "spl_id": "c53d1db5-1c9e-4289-a2a2-961e0dd56f32", "openfda": {"upc": ["0382804109302"], "unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["c53d1db5-1c9e-4289-a2a2-961e0dd56f32"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-109-30)", "package_ndc": "82804-109-30", "marketing_start_date": "20240614"}], "brand_name": "Potassium Chloride Extended-release", "product_id": "82804-109_c53d1db5-1c9e-4289-a2a2-961e0dd56f32", "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": "82804-109", "generic_name": "Potassium Chloride Extended-release", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride Extended-release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214452", "marketing_category": "ANDA", "marketing_start_date": "20210130", "listing_expiration_date": "20261231"}