Package 10135-820-08

{"route": ["ORAL"], "spl_id": "3e780042-e8cd-95fc-e063-6294a90aa28a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["3e78028d-21a0-ba0f-e063-6294a90aac49"], "manufacturer_name": ["Marlex Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 g in 1 BOTTLE (10135-820-08)", "package_ndc": "10135-820-08", "marketing_start_date": "20250801"}], "brand_name": "Potassium Chloride for Oral Solution", "product_id": "10135-820_3e780042-e8cd-95fc-e063-6294a90aa28a", "dosage_form": "SOLUTION", "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": "10135-820", "generic_name": "Potassium Chloride for Oral Solution", "labeler_name": "Marlex Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride for Oral Solution", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "3 g/4.75g"}], "application_number": "ANDA212183", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20261231"}