Package 72789-056-30

{"route": ["ORAL"], "spl_id": "40314483-9bfb-dbb4-e063-6394a90a827c", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["315183"], "spl_set_id": ["cc15ef60-6956-4d34-b86d-72cdd0c0c0bb"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-056-01)", "package_ndc": "72789-056-01", "marketing_start_date": "20200225"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-056-30)", "package_ndc": "72789-056-30", "marketing_start_date": "20230714"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "72789-056_40314483-9bfb-dbb4-e063-6394a90a827c", "dosage_form": "CAPSULE, 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": "72789-056", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "600 mg/1"}], "application_number": "ANDA208864", "marketing_category": "ANDA", "marketing_start_date": "20200102", "listing_expiration_date": "20261231"}